ClinicalTrials.gg
CompletedNCT07866352UAC-DCCUpdated Oct 8, 2026

Uterine-Angle Clamping During Delayed Cord Clamping at Cesarean Delivery

An interventional study of Temporary Uterine-Angle Clamping in Maternal Blood Loss During Cesarean Delivery, sponsored by Baskent University. Completed at 1 site in Turkey (Türkiye). Open to female participants. Per ClinicalTrials.gov, last updated 2026-10-08.

Sponsored by Baskent University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Sep 2025, registered Sep 2026).
Updated Oct 8, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
248
Allocation
Randomized
Sex
Female
01

Study summary

This randomized controlled study evaluated whether temporary clamping of the lateral angles of the uterine incision during a standardized 60-second delayed umbilical cord-clamping period reduces maternal blood loss in women undergoing planned term cesarean delivery. Participants were randomized in a 1:1 ratio to uterine-angle clamping or control. Both groups underwent 60-second delayed cord clamping. Maternal blood loss was assessed using calculated estimated blood loss based on preoperative and 24-hour postoperative hematocrit values.

02

Conditions studied

  • Maternal Blood Loss During Cesarean Delivery
03

In context

Lead sponsor

Baskent University is the lead sponsor of 209 studies on the registry; 35 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

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

  • Singleton pregnancy
  • Planned cesarean delivery at 37+0 to 39+6 weeks of gestation
  • Cesarean delivery before the onset of labor

Exclusion criteria

Exclusion Criteria:

  • Active labor
  • Induction of labor
  • Intrapartum or emergency cesarean delivery
  • Placenta previa
  • Placental abruption
  • Preterm or prelabor rupture of membranes
  • Preeclampsia
  • Chorioamnionitis
  • Chronic systemic disease
  • Known bleeding or coagulation disorder
  • Platelet count \<100,000/mm3
  • Myoma in the lower uterine segment
  • Significant adhesions likely to affect surgery
  • Previous cesarean delivery with a uterine incision other than a Kerr incision
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
248 participants (actual)

Study arms

  • Experimental
    Uterine-Angle Clamping

    Immediately after fetal delivery and while the placenta remained in situ, both lateral angles of the uterine incision were temporarily clamped with ovarian clamps. The umbilical cord was clamped and cut 60 seconds after birth. The clamps were removed when closure of the uterine incision was initiated after placental delivery.

    Procedure: Temporary Uterine-Angle Clamping

  • No intervention
    Control

    Participants underwent 60-second delayed umbilical cord clamping without application of clamps to the uterine incision angles. All other aspects of the surgical technique were identical to those used in the intervention group.

Interventions

  • ProcedureTemporary Uterine-Angle Clamping

    Temporary mechanical clamping of both lateral angles of the low transverse uterine incision during the 60-second delayed cord-clamping interval.

06

What researchers measure

Primary outcomes

  1. Calculated Estimated Blood Loss (cEBL)

    Maternal blood loss calculated using the Stafford method from estimated maternal pregnancy blood volume and the proportional change between preoperative and 24-hour postoperative hematocrit.

    Time frame: within 24 hours after cesarean delivery

Secondary outcomes

  1. Change in Hemoglobin Concentration

    Difference between preoperative and 24-hour postoperative hemoglobin concentration.

    Time frame: Baseline ( preoperative)and 24 hours after cesarean delivery

  2. Change in Hematocrit

    Difference between preoperative and 24-hour postoperative hematocrit.

    Time frame: Baseline ( preoperative ) and 24 hours after cesarean delivery

  3. Calculated Estimated Blood Loss of at Least 500 mL

    Proportion of participants with calculated estimated blood loss of at least 500 mL.

    Time frame: 24 hours after cesarean delivery

  4. Calculated Estimated Blood Loss of at Least 1000 mL

    Proportion of participants with calculated estimated blood loss of at least 1000 mL.

    Time frame: 24 hours after cesarean delivery

  5. Blood Transfusion Requirement

    Requirement for maternal blood transfusion.

    Time frame: From cesarean delivery until hospital discharge, up to 7 days postpartum

  6. Operation Duration

    from cesarean delivery through 24 hours postpartum

    Time frame: During cesarean delivery

  7. Umbilical Artery pH

    Umbilical artery pH measured after delivery.

    Time frame: At delivery

  8. Neonatal Intensive Care Unit Admission

    Admission of the neonate to the neonatal intensive care unit.

    Time frame: from birth until hospital discharge, up to 7 days after birth

  9. Length of Hospital Stay

    Maternal length of hospital stay in days.

    Time frame: From cesarean delivery until hospital discharge, up to 7 days postpartum

07

Study locations

1 site
  • Baskent University Adana Dr. Turgut Noyan Application and Research Center
    Adana, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 8, 2026
Show all 1 update
  1. Oct 8, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07866352
Lead sponsor
Baskent University
Responsible party
MEHMET MURAT ISIKALAN (Associate Professor of Obstetrics and Gynecology, Perinatology Specialist, Baskent University) — Principal investigator
First posted
Oct 8, 2026
Start date
Sep 21, 2025
Primary completion
Sep 21, 2026
Completion
Sep 21, 2026
Last update
Oct 8, 2026

Study contacts

Mehmet Murat Isikalan
principal investigator · Baskent University

Oversight

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

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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