Clinical Outcome of Laparoscopic or Robotic Metroplasty for Uterine Isthmocele

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04414670

Enrollment

Registered

2020-06-04

Start date

2020-02-17

Completion date

2021-11-29

Last updated

2022-08-17

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

Conditions

Laparoscopic or Robotic Metroplasty

Brief summary

To evaluate the clinical outcomes of conventional or robotic - laparoscopic metroplasty for uterine isthmocele with the aid of a bending probe.

Interventions

PROCEDUREC/S

laparoscopic or robotic metroplasty

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to No maximum

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
Change of prolonged menstrual bleeding condition	10 years	Symptoms improvement and perioperative complications

Secondary

Measure	Time frame	Description
Change of scar defect size	10 years	Symptoms improvement and perioperative complications

Countries

Taiwan

Outcome results

None listed

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