Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital
Banqiao District, New Taipei, 22050, Taiwan
Completed
NCT Number: NCT04414670
Clinical Outcome of Laparoscopic or Robotic Metroplasty for Uterine Isthmocele
To evaluate the clinical outcomes of conventional or robotic - laparoscopic metroplasty for uterine isthmocele with the aid of a bending probe.
Completed
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Notify MeKey information
Conditions
Age range
20 year and older
Sex eligibility
Female
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- > 20 years of women
- uterine isthmocele status post laparoscopic or robotic metroplasty with a bent uterine sound
Exclusion criteria
- Those underwent traditional open surgery.
Treatment and study plan
C/S
Procedurelaparoscopic or robotic metroplasty
Primary outcomes
-
Change of prolonged menstrual bleeding condition
Time frame: 10 years
Symptoms improvement and perioperative complications
Secondary outcomes
-
Change of scar defect size
Time frame: 10 years
Symptoms improvement and perioperative complications
Sponsors and collaborators
Lead sponsor
Far Eastern Memorial Hospital
Other
Registry information
Important dates
- Study start
- 2020
- Primary completion
- 2021
- Study completion
- 2021
- First posted
- Jun 4, 2020
- Registry last updated
- Aug 17, 2022
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.