Skip to content

Niche Investigated: Closure of Hysterotomy & Evaluation of 3 Suturing Techniques (Running, Interrupted, and Locked)

Niche Investigated: Closure of Hysterotomy & Evaluation of 3 Suturing Techniques (Running, Interrupted, and Locked)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06695793
Enrollment
225
Registered
2024-11-19
Start date
2024-11-01
Completion date
2026-11-01
Last updated
2024-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caesarean Scar Niche

Brief summary

This study aims to explore the impact of three different suturing techniques (Running, Interrupted & Locked) that used to close the uterine incision at the cesarean section on the formation of a cesarean scar niche

Interventions

The first layer of uterine incision will be closed using individual, separate sutures placed at regular intervals along the incision line. Each suture will be tied independently, ensuring adequate apposition of uterine tissue, followed by a second layer of running continuous sutures.

PROCEDURELocked Sutures

The first layer of uterine incision will be closed using continuous sutures placed along the uterine incision, incorporating a locking technique at specified intervals to prevent unraveling. The knots will be securely tied to maintain tissue approximation, followed by a second layer of running continuous sutures.

BIOLOGICALRunning Continuous Sutures

Double layer closure of uterine incision using running continuous suture used to close the uterine incision without interruption, providing seamless tissue approximation throughout the incision length.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

1. Women with a singleton pregnancy scheduled for elective cesarean section 2. Gestational age at the time of cesarean section between 38 and 40 weeks. 3. Willingness to participate in the study and provide informed consent 4. Age between 18 and 35 years old. 5. BMI \<30

Exclusion criteria

1. Known uterine anomalies or previous uterine surgery (e.g, myomectomy, uterine septum resection) 2. Pre-existing medical conditions contraindicating cesarean delivery or affecting uterine healing (e.g., Anemia, Diabetes) 3. Current smokers. 4. Non-cephalic presentation of the fetus. 5. Low-lying anterior wall placenta and placenta previa. 6. Inability to provide informed consent (e.g., cognitive impairment, language barrier) 7. Any condition deemed by the attending physician to pose a risk to the participant or compromise the study's integrity, for example, Patients who will require excessive suturing for further hemostasis or those who require ligation of one or both uterine arteries

Design outcomes

Primary

MeasureTime frameDescription
Presence of caesarean scar niche and its dimensions.6-12 weeks post-cesarean sectionFollow-up visits will be scheduled at 6-12 weeks post-cesarean section to assess caesarean section niche formation using trans-vaginal ultrasound using Samsung Elite with endovaginal probe of frequency 6 - 12 MHz. Trained sonographers, blinded to the participants' suturing group, will perform the ultrasound examinations to evaluate caesarean section niche presence and its dimensions.

Secondary

MeasureTime frame
Operative timeduring operation
Estimate blood lossduring operation

Countries

Egypt

Contacts

Primary ContactAbdalla Moussa
Dr_abdallamousa@yahoo.com+20127664430
Backup ContactSally Collins
sally.collins@wrh.ox.ac.uk+44 7958 656885

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026