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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04825821
Other study ID # BARB-CSCAR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2019
Est. completion date September 30, 2022

Study information

Verified date December 2022
Source Ospedale Policlinico San Martino
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Late sequelae of a cesarean section related to a uterine scar defects include gynecological symptoms and obstetric complications. The aim of this study was to evaluate the incidence and characteristics of cesarean scar defects after uterine closure by double-layer barbed suture.


Recruitment information / eligibility

Status Completed
Enrollment 247
Est. completion date September 30, 2022
Est. primary completion date July 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who underwent elective cesarean section at = 37 weeks of gestation Exclusion Criteria: - Patients who underwent concomitant surgical procedures during the cesarean section (i.e., tubal sterilization); - Patients who underwent a previous abdominal surgery (with exception of appendectomy) including a cesarean section or other laparotomic/laparoscopic uterine surgical procedure (i.e., myomectomy); - Patients who had a previous diagnosis of Mullerian uterine anomalies elective cesarean for the second time or after uterine surgery; - Patients who had evidence of PAS disorders or placenta previa.

Study Design


Intervention

Procedure:
Clinical and ultrasonographic assessment
Routinely assessment by objective examination and transvaginal ultrasonographic scan 6, 12, and 24 months after the surgical procedures

Locations

Country Name City State
Italy IRCCS Ospedale Policlinico San Martino Genoa

Sponsors (1)

Lead Sponsor Collaborator
Ospedale Policlinico San Martino

Country where clinical trial is conducted

Italy, 

References & Publications (3)

Agarwal S, D'Souza R, Ryu M, Maxwell C. Barbed vs conventional suture at cesarean delivery: A systematic review and meta-analysis. Acta Obstet Gynecol Scand. 2021 Jun;100(6):1010-1018. doi: 10.1111/aogs.14080. Epub 2021 Feb 5. — View Citation

Alessandri F, Evangelisti G, Centurioni MG, Gustavino C, Ferrero S, Barra F. Fishbone double-layer barbed suture in cesarean section: a help in preventing long-term obstetric sequelae? Arch Gynecol Obstet. 2021 Sep;304(3):573-576. doi: 10.1007/s00404-021-06121-8. — View Citation

Jordans IPM, de Leeuw RA, Stegwee SI, Amso NN, Barri-Soldevila PN, van den Bosch T, Bourne T, Brolmann HAM, Donnez O, Dueholm M, Hehenkamp WJK, Jastrow N, Jurkovic D, Mashiach R, Naji O, Streuli I, Timmerman D, van der Voet LF, Huirne JAF. Sonographic examination of uterine niche in non-pregnant women: a modified Delphi procedure. Ultrasound Obstet Gynecol. 2019 Jan;53(1):107-115. doi: 10.1002/uog.19049. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of uterine scar defects Number of simple and complex uterine scar defects is evaluated by transvaginal ultrasound 6 months after the cesarean section
Primary Number of uterine scar defects Number of simple and complex uterine scar defects is evaluated by transvaginal ultrasound 12 months after the cesarean section
Primary Number of uterine scar defects Number of simple and complex uterine scar defects is evaluated by transvaginal ultrasound 24 months after the cesarean section
Secondary Residual myometrium thickness (RMT), depth, width and length of uterine scar defects RMT, depth, width, and length are evaluated by transvaginal ultrasound 6 months after the cesarean section
Secondary Residual myometrium thickness (RMT), depth, width and length of uterine scar defects RMT, depth, width, and length are evaluated by transvaginal ultrasound 12 months after the cesarean section
Secondary Residual myometrium thickness (RMT), depth, width and length of uterine scar defects RMT, depth, width, and length are evaluated by transvaginal ultrasound 24 months after the cesarean section
Secondary Number of patients with postmenstrual spotting Number of patients with postmenstrual spotting is evaluated by medical interview 6 months after the cesarean section
Secondary Number of patients with postmenstrual spotting Number of patients with postmenstrual spotting is evaluated by medical interview 12 months after the cesarean section
Secondary Number of patients with postmenstrual spotting Number of patients with postmenstrual spotting is evaluated by medical interview 24 months after the cesarean section
Secondary Number of patients with dysmenorrhea Number of patients with dysmenorrhea is evaluated by medical interview with VAS (visual analogue scale) 6 months after the cesarean section
Secondary Number of patients with dysmenorrhea Number of patients with dysmenorrhea is evaluated by medical interview with VAS (visual analogue scale) 12 months after the cesarean section
Secondary Number of patients with dysmenorrhea Number of patients with dysmenorrhea is evaluated by medical interview with VAS (visual analogue scale) 24 months after the cesarean section
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