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
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%).
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.
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 →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.
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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.
Exclusion Criteria:
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.
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.
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 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 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.
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.
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.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Controls: Healthy pregnant women of the same gestational age with routine physical examinations will be enrolled as a control group.
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
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
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
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
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
Change in pruritus of the visual analog scale (VAS) at delivery.
Pruritus will be measured on 0-100mm scale.
Time frame: At delivery
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
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
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
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
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
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
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
Plan to share: No
No publications or documents are linked to this record.
Started Dec 2022 (actual). Primary completion is estimated for Jul 2026, 43 months after the start.
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Intrahepatic Cholestasis of Pregnancy →
Post Graduate Institute of Medical Education and Research, Chandigarh →