Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
FEMALE
Healthy Volunteers
NCT05312775

Niche In CEsarean Scar Trial (NICEST)

Led by Nguyen Thi Thu Ha · Updated on 2024-03-01

938

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Rationale: Cesarean delivery (CD) rates are increasing rapidly worldwide. The consequences of cesarean section not only affect the next pregnancies such as uterine rupture or malplacentation but also cause many gynecological complications or infertility due to the formation of cesarean scar defect (CSD) or Niche. One of the major factors for Niche formation is the techniques of hysterotomy closure at the time of cesarean delivery. Most common hysterotomy closures include single and double layers closure. However, there is limited literature to prove which technique decreases niche creation and associated gynecological complications. Objective: To compare the effect of uterine closure techniques during CD on the formation of Niche evaluated on transvaginal ultrasound and gynecological complications. Study design: a double-blinded, single-center, randomized clinical trial. Setting: Hanoi Obstetrics \& Gynecology Hospital (HOGH), Viet Nam. Study population: All women at gestational age ≥ 37 0/7 weeks who undergo a primary CD (planned or unplanned). Intervention: After informed consent, women will be randomized to either unlocked single layer closure or unlocked double-layer closures of cesarean uterine scar in a 1:1 ratio Primary outcome: The proportion of Niche over time (at 6, 12, 18, 24 months after CD) in the two groups. Power calculation: A sample size of 389 women is needed for each group. Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: Both uterine closure methods followed by the Vietnam Ministry of Health (VN-MOH), transvaginal ultrasound is also not harmful. It is believed that there are no potential increased risks to patients taking part in this trial because of the standard care and management they receive.

CONDITIONS

Official Title

Niche In CEsarean Scar Trial (NICEST)

Who Can Participate

Age: 18Years - 60Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women undergoing their first cesarean delivery, planned or unplanned
  • Age 18 years or older
  • Gestational age of 37 weeks or more
Not Eligible

You will not qualify if you...

  • Previous major uterine surgery such as laparoscopic or open fibroid removal or septum resection
  • Abnormal menstrual bleeding caused by conditions like cervical dysplasia, hydrosalpinx, uterine anomalies, endocrine disorders affecting ovulation, or presence of polyps or fibroids
  • Presence of painful menstrual symptoms such as dysmenorrhea, painful intercourse, or suprapubic pain
  • Abnormal placenta conditions in the current pregnancy such as placenta previa or placenta percreta

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hanoi Obstetrics and Gynecology Hospital

Hanoi, Hanoi, Vietnam, 100000

Actively Recruiting

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Research Team

H

Ha TT Nguyen, PhD.MD

CONTACT

G

Giang TT Duong, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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