ClinicalTrials.gg
RecruitingNCT05691036ICPUpdated May 18, 2026

Bile Acids Metabolism and Genetic Mutation Profile in the Intrahepatic Cholestasis of Pregnacy in Indian Population

An observational study in Intrahepatic Cholestasis of Pregnancy, Genetic Mutation and Health Related Quality of Life, sponsored by Post Graduate Institute of Medical Education and Research, Chandigarh. Recruiting at 1 site in India. Open to female participants aged 21 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-18.

Sponsored by Post Graduate Institute of Medical Education and Research, Chandigarh · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started Dec 2022; still recruiting 3 years 11 months later.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
150
Ages
21 Years to 45 Years
Sex
Female
01

Study summary

Intrahepatic cholestasis of pregnancy (ICP) is a disorder characterized by itching, elevated fasting serum bile acids ≥10μmol/L (and elevated serum transaminases), with increased risks of perinatal complications, including spontaneous preterm labor, fetal distress, infant respiratory distress syndrome, meconium-stained liquor (MSL), and sudden intrauterine death (IUD). The Incidence of ICP varies from 0.1 to 15.6% of all pregnancies, with the highest cases in Chile, South Asia, America, and Scandinavia. The burden of ICP in India according to various states is as follows Punjab (3.1%), Chandigarh (4.8%), Delhi (0.79%), West Bengal (3.3%), and Lucknow (Uttar Pradesh) (2.8%).

Read the detailed description

Many physiological, anatomical, and hormonal changes occur in the body during pregnancy to facilitate the best possible growth of the fetus. A functional liver and bile acids (BA) milieu are critical for the development of the fetus, and adverse pregnancy outcomes are possible in women who have primary liver disease. Some pre-existing hepatobiliary diseases may be diagnosed incidentally during pregnancy, such as chronic viral hepatitis. Some common pregnancy-related liver diseases are Intrahepatic Cholestasis of pregnancy (ICP), hemolysis elevated liver enzymes and low platelets (HELLP) syndrome, and acute fatty liver of pregnancy (AFLP). ICP is a cholestatic disorder characterized by (i) pruritus, with onset in the second and third trimester of pregnancy, without any primary skin lesions, (ii) elevated fasting serum bile acids ≥10μmol/L (and elevated serum transaminases), (iii) spontaneous relief of signs and symptoms within two to three weeks after delivery, and (iv) absence of other diseases that cause pruritus and jaundice. Many studies have attempted to associate maternal serum bile acids/ total bile acids with adverse fetal outcomes. ICP is associated with increased risks of perinatal complications, including spontaneous preterm labor, fetal distress, infant respiratory distress syndrome, meconium-stained amniotic fluid, and sudden intrauterine death (IUD). Recent data suggest that women with jaundice had higher rates of prenatal abnormalities than women with just pruritus in ICP. Pruritus can appear as early as seven weeks without causing a rash. Itching is usually noticed early on the palms of the hands and the soles of the feet, although it can occur everywhere on the body. Other symptoms of ICP include dark urine, increased clotting time, fatigue, nausea, loss of appetite, jaundice, and discomfort in the upper right quadrant of the abdomen. It may be mild and tolerable for some patients but may also be very severe and disabling. Women with ICP develop mild jaundice and subclinical steatorrhea. Jaundice typically develops 1 to 4 weeks after the onset of pruritus. Subclinical steatorrhea with fat malabsorption leads to vitamin K deficiency resulting in prolonged prothrombin time and postpartum hemorrhage.

The incidence and prevalence of ICP vary with ethnicity and geography. Ethnic distribution of ICP as Caucasian (53.6%), South Asian (22.6%), African (0.6%), Asian (8.4%), and Australian (3.8%) were noted (8). Among the Asians, Asian of Indian origin 1.24%, Pakistan origin of 1.46%, and whites of 0.62% were found to show Indians and Pakistan origin of Asian have a higher prevalence than whites. Concerning the geographic distribution of ICP, the Incidence of ICP varies from 0.1 to 15.6% of all pregnancies, with the highest cases in Chile, South Asia, America, and Scandinavia. In the case of individual countries such as Chile, 9%, Canada, 0.07%, China, 0.32%, and North California, 1.9% incidence were reported. It is more common in South America as compared to other northern European continents. The incidence of ICP was reported as 0.5-1.5% of pregnancies in Finland. As this study will be done among the Indian population, the burden of ICP in India is reported as Punjab at 3.1%, Chandigarh at 4.8%, Delhi at 0.79%, Nepal at 1.1.5%, West Bengal at 3.3%, Lucknow 2.8%, indicating an urgent need to focus and find out cost-effective and early prognosis and diagnosis of ICP.

ICP is a multifactorial disease interplay between genetic, environmental, and hormonal factors. Common risk factors are the history of oral contraceptive pill (OCP) use, twins, selenium deficiency, genetic transporters defects, and recurrence in the subsequent pregnancy. Patients are usually diagnosed in the second and third trimesters, with increased incidence in winter. Genetic factors contribute as risk factors for ICP including mutation in ATP binding cassette family as ATP binding cassette subfamily B member 4(ABCB4), ATP-binding cassette, sub-family B member 11(ABCB11), ATPase Phospholipid Transporting 8B1(ATP8B1), ATP Binding Cassette Subfamily C Member 2(ABCC2), and tight junction protein 2(TJP2) genes. Bile mainly consists of bile salt, organic anions, electrolytes, phosphatidylcholine, and cholesterol. These components are transported by active process against the concentration gradient by specific transporters such as bile salt export pump (BSEP), Sodium taurocholate co-transporting polypeptide (NTCP), major transporter for the secretion of bile acids from hepatocytes into bile in humans. A study on deoxyribonucleic acid (DNA) of the Italian population with the help of polymerase chain reaction (PCR) and automated sequencing. They found five novel variants of mutation in ABCB4 and ABCB11 and confirmed the statistically significant susceptibility to ICP. Environmental factors associated with ICP include seasonal variation, selenium deficiency, and vitamin D deficiency. Hormonal factors such as estrogen level, sulfated progesterone, intake of oral contraceptive pills, and second-trimester hormonal changes in pregnant women can be attributed as risk factors for ICP. In the urine of pregnant women with ICP, sulfated progesterone correlates with the severity of ICP. Apart from these, other risk factors are responsible for ICP, and they found a statically significant association between pregestational diabetes, tobacco use, history of cholecystectomy, history of ICP in a previous pregnancy, and pregnancy-induced hypertension (PIH).

Placental expression of genes due to placental hypoxia and proteins related to apoptosis, oxidative stress, lipid metabolism, cell proliferation, and immunological response are associated with ICP. Increased total serum BAs and changes in BAs profile reverse the transplacental BA(bile acids) gradient, and increased inflammatory cytokines like interleukin 4(IL4), interleukin 6(IL6), interleukin 12 (IL12), and tumor necrosis factor(TNF) cause respiratory distress in infants and preterm delivery. Immune response, vascular endothelial growth factor(VGEF)signaling pathway, and G-protein-coupled receptor signaling were the most common regulatory genes responsible for inflammatory response, vasculogenesis, and angiogenesis, all essential in ICP pathogenesis. Autotaxin (ATX) is lysophosphatidic acid (LPA) essential for angiogenesis and neuronal development during embryogenesis, cellular motility, proliferation, and lymphocyte homing. ATX levels are reported to be increased during pregnancy and correlate positively with gestational age. LPA and ATX levels were significantly higher in ICP. A large prospective study in Sweden revealed severe perinatal outcomes of ICP as spontaneous preterm labor, asphyxia events, meconium staining of amniotic fluid, and placental and membrane changes did not occur until the level of serum bile acid reached>40umol/L. ICP is a pregnancy-related disorder that is expected to resolve after delivery. However, population-based cohort studies revealed that ICP acts as a risk factor for hepatobiliary disease even after the completion of pregnancy. A significant association between hepatitis C virus (HCV), non-alcoholic liver disease, gallstone, and cholelithiasis, with increased risk of non-alcoholic pancreatitis in women, was observed in women with ICP. A population-based cohort study, with an of 0.32%-0.58% of ICP in Sweden, gives a significant risk association of ICP with gestational diabetes, pre-eclampsia, and a nonsignificant association with postpartum hemorrhage. Total serum bile acids >40mmol/l as severe ICP and associated with increased risk of gestational diabetes mellitus(GDM), pregnancy-induced hypertension(PIH) was reported and managed with ursodeoxycholic acid (UDCA).

Some therapeutic agents such as ursodeoxycholic acid(UDCA), rifampicin, antihistaminic drugs, vitamin K and some topical emollients have been used to alleviate nocturnal pruritus/ pruritus in ICP. Some trials related to reducing the adverse perinatal outcome of ICP were done with the administration of UDCA, dexamethasone, cholestyramine, S-adenosyl methionine(SAMe), plasmapheresis, and fish supplements. UDCA is currently the most effective therapeutic agent used in clinical practice to manage ICP. Several meta-analyses with observational studies or randomized trials have been done on the effectiveness of UDCA, but the results are equivocal. Dexamethasone, rifampicin, SAMe, and cholestyramine also have some roles in the management of ICP. However, reducing pruritus and other adverse perinatal outcomes in pregnancy is unclear. UDCA was effective in improving clinical presentation, normalization of serum profile, and a significant reduction in meconium staining, spontaneous birth, or fetal distress compared to the control/ placebo group. Maternal total serum BAs are significantly associated with reduced infant size and are small for gestational age. Since ICP is the most typical pregnancy-related liver disorder, has multifactorial risk factors, has unclear etiopathogenesis, and results in adverse perinatal outcomes. Pruritus may considerably impair the patient's quality of life as a pregnant woman, causing sleep deprivation and psychological suffering. Only a few studies have been done in India concerning ICP, most of which are related to the reference range of total BAs and the prevalence of ICP. There is no Indian data on how ICP affects the quality of life of a pregnant woman or prospective assessment of genetic risk and bile acid metabolism. So, the aim is to determine the bile acid profile and related metabolites in serum, identify prognostic markers of ICP and assess related risk factors, including the effect of medication and the quality of life of patients with ICP. This research will prospectively evaluate perinatal outcomes and genetic risk factors, which have a bearing on neonatal health. Keeping in mind the symptoms and severity of pruritus, the factors affecting the disease course of pregnant women suffering from ICP will also be evaluated.

02

Conditions studied

  • Intrahepatic Cholestasis of Pregnancy
  • Genetic Mutation
  • Health Related Quality of Life

Keywords

  • Intrahepatic cholestasis of pregnancy
  • Genetic Mutations in pregnancy associated cholestasis
  • Pruritus
03

In context

Intrahepatic Cholestasis of Pregnancy

26 studies on the registry are indexed under Intrahepatic Cholestasis of Pregnancy; 10 are open to participants now.

This study's planned enrollment of 150 is above the median of 118 across 18 observational studies indexed under Intrahepatic Cholestasis of Pregnancy.

Browse Intrahepatic Cholestasis of Pregnancy studies →

Lead sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh is the lead sponsor of 298 studies on the registry; 45 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Study Population:

Group 1: Pregnant women with ICP, n= 75 Cases: Pregnant women with consistent pruritus or on medication for pruritus associated with an elevated level of serum transaminase (ALT>40 IU/L or AST >37 IU) and raised serum bile acids ≥10μmol/L will be eligible for inclusion in the study.

Group 2: Pregnant women without ICP, n=75 Controls: Healthy pregnant women of the same gestational age with routine physical examinations will be enrolled as a control group.

Setting: PGIMER (Chandigarh, India)

Study Centre - Departments of Hepatology/ Obstetrics and Gynaecology, PGIMER, Chandigarh

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age > 21 years with consistent pruritus
  • Characterized by consistent pruritus associated with elevated levels of serum transaminases ( > 40 U/L or AST > 37 U/L) or raised total serum bile acids (≥ 10 µmol/L)
  • Able to understand and comply with the requirements of the study and voluntarily agrees to participate in the study by giving written before any study-related activity is performed
  • Voluntary informed consent to participate until their delivery and also willing to be followed until their delivery
  • Agrees to provide information on perinatal and maternal outcomes at or after delivery

Exclusion criteria

Exclusion Criteria:

  • Viral and Infectious diseases such as virus (HBV), virus (HCV) related liver disease, Epstein Barr virus (EBV), Cytomegalovirus (CMV), (HIV) infection) hepatitis C virus (HBV), hepatitis E virus (HEV)
  • Primary dermatologic diseases associated with pruritus
  • Metabolic diseases (including alcohol abuse)
  • Other causes of cholestasis (i.e., primary biliary cholangitis (PBC); primary sclerosing cholangitis (PSC)
  • liver disease
  • Obstructive biliary diseases
  • Cholestatic drug-induced liver injury
  • Clinical severe conditions that may affect outcomes include heart failure, renal failure, primary cardiopulmonary diseases
  • Twins and triplet pregnancy
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
150 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Pregnant women with ICP

    Case: Pregnant women with consistent pruritus or on medication for pruritus associated with an elevated level of serum transaminase alanine transaminase(ALT)\>40 IU/L or aspartate transaminase(AST)\>37 IU) and raised serum bile acids ≥10µmol/L will be eligible for the inclusion in the study.

  • Pregnant women without ICP

    Controls: Healthy pregnant women of the same gestational age with routine physical examinations will be enrolled as a control group.

06

What researchers measure

Primary outcomes

  1. Profile of serum bile acids (conjugated and unconjugated) in patients with ICP (Intrahepatic cholestasis of pregnancy) and without ICP.

    Bile acids profiling will be accessed by using liquid chromatography combined with mass spectrometry (LC-MS/MS)

    Time frame: At Enrolment

  2. Change in the profile of serum bile acids (conjugated and unconjugated) in patients with ICP (Intrahepatic cholestasis of pregnancy) and without ICP.

    Bile acids profiling will be accessed by using liquid chromatography combined with mass spectrometry (LC-MS/MS)

    Time frame: At Delivery

Secondary outcomes

  1. Mode of delivery in the cohort of women with ICP.

    During follow-up, delivery-related details such as mode of delivery, any postpartum hemorrhage or requirement for blood transfusion, gestational age at delivery, an indication of cesarean section, mode of induction of labor, duration of stages of labor and their association with intrahepatic cholestasis of disease and frequency in comparison to control/apparently healthy pregnant women.

    Time frame: At delivery

  2. Assessment of newborn physical and clinical profile.

    Details related to newborns such as birth weight (in kg), height (in cm) and APGAR score, along with any adverse perinatal outcome such as stillborn, respiratory such as respiratory distress, fetal cardiac dysfucntion and other clinical condition will also be recorded and compared with apparently healthy control pregnant women.

    Time frame: At delivery

  3. At the baseline visit, measurement of pruritus of the visual analog scale (VAS).

    Pruritus will be measured on 0-100mm scale.

    Time frame: Day 0

  4. Change in pruritus of the visual analog scale (VAS) at delivery.

    Pruritus will be measured on 0-100mm scale.

    Time frame: At delivery

  5. Measurement of fasting bile acids, liver function test(LFT) at baseline in pregnant women with ICP.

    Fasting bile acids, liver function test

    Time frame: Day 0

  6. Change in fasting bile acids, liver function test(LFT) in pregnant women with ICP.

    Fasting bile acids and liver function test

    Time frame: At delivery

  7. Association of ICP with other co-morbid diseases such as pregnancy-induced hypertension, fatty liver of pregnancy, gestational diabetes, etc.

    Other liver related disease with ICP will be assessed

    Time frame: day 0

  8. Pedigree analysis concerning family history of ICP.

    ICP is genetic, history of ICP will be assessed among the mother and sister sibling of ICP patients

    Time frame: Day 0

  9. The baseline profile of serum bile acids (conjugated and unconjugated) in patients with Intrahepatic cholestasis of pregnancy(ICP) and without ICP.

    Bile acids profiling will be accessed by using liquid chromatography combined with mass spectrometry (LC-MS/MS)

    Time frame: Day 0

  10. Role of ABCB11, ABCB4, and ATP8B1 gene mutations in women with ICP

    Targeted Next Generation sequencing will be done at baseline

    Time frame: Day 0

  11. The HRQOL (Health-related quality of life) in patients with ICP and healthy pregnant women.

    Short form (SF) health survey questionnaire will be used to access the quality of life in ICP patients. SF-36 is a 36 Item questionnaire, with a range of 0-100, and a mean score of 50. A higher score indicates a better health-related quality of life.

    Time frame: Day 0

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Dec 2022 (actual). Primary completion is estimated for Jul 2026, 43 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 1, 2022
First posted
Jan 19, 2023
StartActual
Dec 8, 2022
Primary completionEst.
Jul 2026
CompletionEst.
Jul 2026
Last update
May 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05691036
Responsible party
Madhumita Premkumar (ASSOCIATE PROFESSOR, Post Graduate Institute of Medical Education and Research, Chandigarh) — Principal investigator
First posted
Jan 19, 2023
Start date
Dec 8, 2022
Primary completion
Jul 2026 (estimated)
Completion
Jul 2026 (estimated)
Last update
May 18, 2026

Study contacts

Dr Madhumita Premkumar, DM
Contact
drmadhumitap@gmail.com
7087003409
Jasvinder Nain, MPH
Contact
jasvindernain1506@gmail.com
Madhumita Premkumar
principal investigator · PGIMER, Chandigarh

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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