Uterine Inertia clinical trials
The registry lists 39 studies for Uterine Inertia across more than 10 countries. 7 are recruiting or about to start. 16 of them are mainly about Uterine Inertia (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-06.
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Who runs them
Stanford University (3) · Baylor Research Institute (3) · Brigham and Women's Hospital (2) · Gynuity Health Projects (2) · Maisonneuve-Rosemont Hospital (2) · Kanuni Sultan Suleyman Training and Research Hospital (2) · University of Saskatchewan (1) · NYU Langone Health (1)
What is being tested here
Drugs under test in Uterine Inertia studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Calcium Gluconate | 2 | 0 | 2 |
| Oxytocin | 1 | 0 | 5 |
| Methylergonovine | 0 | 0 | 4 |
| Misoprostol | 0 | 1 | 4 |
| Calcium Chloride | 0 | 1 | 2 |
| Carbetocin | 0 | 0 | 2 |
| Carboprost | 0 | 0 | 1 |
| Tranexamic Acid | 0 | 0 | 1 |
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 3
- Dec 2026Balloon Tamponade Versus Gauze Packing for Postpartum Hemorrhage · Khyber Teaching Hospital
- Jun 2027Comparison of Effect of Two Different Doses of Intravenous Oxytocin on Patients Undergoing Elective Cesarean Section · Shalamar Hospital
- Oct 2027Administration Of Calcium Gluconate for The Reduction of Blood Loss During Vaginal Delivery · Rambam Health Care Campus
Who these studies take
Of the 3 Uterine Inertia studies recruiting now, 2 (67%) set no upper age limit and 1 (33%) stop at 75 or younger. 0 (0%) take children under 18. 2 (67%) are for women only and 1 (33%) for men only; 1 (33%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 0 (0%) | 0 (0%) |
| 18 | 2 (67%) | 1 (33%) |
| 30 | 2 (67%) | 1 (33%) |
| 40 | 2 (67%) | 1 (33%) |
| 50 | 1 (33%) | 1 (33%) |
| 65 | 1 (33%) | 1 (33%) |
| 75 | 1 (33%) | 1 (33%) |
| 85 | 1 (33%) | 1 (33%) |
Across all 39 studies, recruiting or not: 51% stop at 75 or younger and 51% at 65; 26% take children; 95% are for women only and 3% for men only; 51% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
What changed recently
From the registry's own updates since Oct 14, 2026.
Newly registered1
Studies
Recruiting first, then most recently updated. Showing 39 of 39. search them.
- Comparison of Effect of Two Different Doses of Intravenous Oxytocin on Patients Undergoing Elective Cesarean SectionNot yet recruitingNCT07922083Not applicable
- Carbetocin Monotherapy Versus Carbetocin Plus Oxytocin Infusion in Elective Cesarean Delivery: A Non-Inferiority TrialRecruitingNCT07636421Phase 41 country
- Oxytocin Bolus Versus Infusion in High-Risk Patients Undergoing Elective Cesarean Section (INBOX-HR)Not yet recruitingNCT07688512Phase 4
- Prophylactic Intravenous Calcium Gluconate to Decrease Blood Loss at Time of Cesarean Delivery in Pregnant Patients at High Risk for Uterine AtonyRecruitingNCT07217899Phase 21 country
- Administration Of Calcium Gluconate for The Reduction of Blood Loss During Vaginal DeliveryRecruitingNCT07714902Not applicable1 country
- Balloon Tamponade Versus Gauze Packing for Postpartum HemorrhageNot yet recruitingNCT07609589Not applicable
- Exteriorization Versus In Situ Hysterotomy Repair During Cesarean: Effects on Uterine ToneNot yet recruitingNCT07606846Not applicable
- Placental Removal Method And Uterine Massage On Preventing Postpartum HemorrhageCompletedNCT061928361 country
- Cooling the Uterus in C-section After Dysfunctional LaborTerminatedNCT02910115Not applicable
- Exploration and Determination of Genomic Markers Predictive of Uterine AtonyCompletedNCT034139171 country
- LXRs, Cholesterol Metabolism and Uterine DystociaTerminatedNCT011071581 country
- Temporary Aortic Occlusion With the Abdominal Tourniquet for Refractory Postpartum Haemorrhage: A Proof-of-Concept Study in a War-Affected RegionCompletedNCT07016568Not applicable1 country
- Second-Line Uterotonics in Postpartum Hemorrhage: A Randomized Clinical TrialCompletedNCT03584854Phase 41 country
- Questionnaire for Obstetricians and AnesthesiologistActive, not recruitingNCT050897211 country
- Calcium Chloride for Prevention of Blood Loss During Intrapartum Cesarean DeliveryCompletedNCT05027048Phase 31 country
- Multimodal Uterotonics at the Time of Cesarean Section in Laboring PatientsCompletedNCT03904446Phase 41 country
- Calcium Chloride for Prevention of Uterine Atony During CesareanCompletedNCT03867383Phase 1/21 country
- Novel Approach of Hayman Uterine Compression Sutures for Management of Severe Atonic Postpartum Hemorrhage: Three Vertical SuturesCompletedNCT046901531 country
- Prediction of Uterine Atony After Vaginal Delivery by ElastographyCompletedNCT042677831 country
- Intravenous Versus Intramuscular Administration of Methylergonovine for Uterine Contraction in Cesarean SectionsWithdrawnNCT03303235Early Phase 11 country
- The Comparison of the Effect of Different Oxytocin Administrations on the Blood Loss During Cesarean DeliveryCompletedNCT03967171Not applicable1 country
- Database Evaluating Outcomes of Using Carbetocin as the Primary Uterotonic Following Cesarean DeliveryCompletedNCT039594361 country
- Serum Antimullerian Hormone Levels in Patients Who Underwent Hayman SutureStatus unknownNCT039304071 country
- A Novel Technique Of Uterine Cooling During Repeated Cesarean Section For Reducing Blood LossCompletedNCT03793153Not applicable1 country
- Serum Antimullerian Hormone Levels in Patients Who Underwent Uterine Artery LigationCompletedNCT038962431 country
- Oxytocin Dosing at Planned Cesarean Section and AnemiaWithdrawnNCT03361124Phase 4
- Buccal Misoprostol During Cesarean Section for Preventing Postpartum HemorrhageCompletedNCT01733329Phase 41 country
- Uterine Cooling During Cesarean Delivery to Reduce Blood Loss and Incidence of Postpartum HemorrhageCompletedNCT02229513Not applicable1 country
- An Evidence Based Protocol for Oxytocin Administration in Vaginal DeliveryWithdrawnNCT02410655Phase 4
- Oxytocin And Uterotonic Agent Use For Cesarean DeliveryCompletedNCT01549223Phase 41 country
- Treatment of Postpartum Hemorrhage With Misoprostol: Fever StudyCompletedNCT02163616Phase 31 country
- Role of Tranexamic Acid Versus Uterine Cooling at Caesarean SectionCompletedNCT02780245Phase 41 country
- Oxytocin Regimen to Prevent Atony and Postpartum Hemorrhage During Vaginal Delivery: 3-arm RCTCompletedNCT00790062Phase 41 country
- Comparative Study on the Effects of Sublingual Misoprostol in Addition to Standard AMTSL in Low Risk Parturients in LASUTH, Ikeja.Status unknownNCT02424201Early Phase 1
- Comparison of Two Doses of Carbetocin for Prevention of Uterine Atony, During Elective Cesarean SectionCompletedNCT01630187Phase 41 country
- ED90 Determination of Carbetocin for the Prevention of Uterine Atony in Women Undergoing an Elective Cesarean DeliveryStatus unknownNCT01579201Phase 41 country
- Does Intramyometrial Oxytocin Improve Outcome in Elective Cesarean Delivery?WithdrawnNCT01252342Phase 41 country
- Up-Down Oxytocin InfusionCompletedNCT00785395Phase 41 country
- Fever After Misoprostol Administration for the Treatment of Primary Postpartum HemorrhageCompletedNCT01080846Not applicable1 country