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Laparoscopic Repair of Cesarean Scar Niche

Laparoscopic Repair Of Cesarean Scar Niche: Randomized Controlled Trial.

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04307524
Enrollment
30
Registered
2020-03-13
Start date
2020-03-15
Completion date
2021-03-30
Last updated
2020-03-13

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

Conditions

Cesarean Section Complications

Keywords

cesarean scar niche

Brief summary

Evaluation of laparoscopy repair of cesarean scar niche in resolution of symptoms related to niche as compared to expectant management.

Detailed description

Recently, The percentage of Cesarean section (CS) deliveries has dramatically increased in most countries. The presence of a niche at the site of a CS scar has been observed. A niche is mainly a sonographic finding defined as a triangular anechoic area at site of incision. ( Mascarello et al, 2017) Alternative terms for a niche are Cesarean scar defect (Wang et al, 2009), deficient Cesarean scar (Ofili-Yebovi et al, 2008), diverticulum (Surapaneni et al, 2008), pouch (Fabres el al, 2003) and isthmocele. (bogres el al, 2010) As not all women with previous CS develop a niche, it is a matter of interest to identify the risk factors that may predict their development. (Sholapurkar , 2018) Possible causes of this condition may be surgery or patient related. Surgery related factors as low cervical incision, incomplete closure of the uterus (decidual sparing) and inadequate hemostasis. Patient related factors may be attributed to infection. ( Vervoort et al, 2015) Cesarean scar niche may be asymptomatic or may cause a number of obstetrical and gynecological problems (cesarean scar syndrome) . ( Vervoort et al,2015b) Obstetrical complications of the niche are cesarean scar ectopic pregnancy, placenta previa and morbidly adherent placenta, cesarean scar dehiscence following incomplete abortion secondary to uterotonic drugs, Scar dehiscence and tender scar even scar rupture (Tanimura el al, 2015) Gynecological symptoms of the niche are postmenstrual spotting, Intermenstrual bleeding, Dysmenorrheal, Dysparunia and secondary infertility. (Tanimura el al, 2015) Various methods to detect and measure a niche have been described. The majority of papers have evaluated the niche with the use of transvaginal sonography (TVS) (Vaate et al, 2011), and contrast-enhanced sonohysterography (SHG) (Bij de Vaate et al, 2011), but a minority have used hysteroscopy (El-Mazny et al, 2011) or hysterosalpingography. (Surapaneni and Silberzweig, 2008 ) At present there is no consensus regarding the gold standard for the detection and measurement of a niche. (Vaate et al, 2014) Symptomatic cesarean scar niche (cesarean scar syndrome) can be managed conservatively using combined oral contraceptive pills especially in women not seeking fertility, or it can be treated using minimal invasive surgery as hysteroscopic resection (vervoot et al,2017) , laparoscopic repair (ma et al,2017) or vaginal repair (Yao, 2014) In this study we will evaluate laparoscopic management of cesarean scar niche

Interventions

laparoscopic suture repair of cesarean scar niche

DRUGmedical treatment in the form of combined hormonal contraception

patient will receive for three months daily without interruption, no pill-free interval drug names is Genera BAYERhealthcare

Sponsors

Zagazig University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

computer-generated sequence

Intervention model description

randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

1. History of cesarean section. 2. Postmenstrual and/or intermenstrual spotting. 3. Cesarean scar niche of at least 2 mm in depth diagnosed by saline infusion sonography

Exclusion criteria

1. pregnancy 2. Uterine anomalies 3. Hysterotomy. 4. history Placenta previa and MAP 5. Upper segment incision, Vertical uterine incision 6. submucosal fibroids 7. adenomyosis. 8. History atypical endometrial cells, cervical dysplasia, 9. cervical or pelvic infection. 10. Irregular cycle. 11. lactation amenorrhea.

Design outcomes

Primary

MeasureTime frameDescription
post-menstrual spotting6 month after interventionnumber of days of post-menstrual spotting spotting or bleeding after 8 days of menstruation whatever the amount

Secondary

MeasureTime frameDescription
menstrual related pain6 month after interventiondegree of menstrual related pain as descriped by the patient on Visual Analogue Scale of pain from 1 to 10
infertility6 month after interventionfailure of conception despite regular sexual intercourse within 6 months from intervention or stopping gynera

Outcome results

None listed

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