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Clinical Trials in China / NCT06244251
Active, not recruiting Not applicable

Comparison Between Laparoendoscopic Single-site Surgery and Multi-port Laparoscopy in Treating Uterine Fibroids

NCT06244251 · tracked via the Priya Life Science China tracker
Sponsor
West China Second University Hospital
Phase
Not applicable
Started
2023-06-24
Last updated
2024-02-06

Condition(s) studied

Uterine FibroidUterine SarcomaUterine Leiomyosarcoma

Investigational drug(s) / intervention(s)

TU-LESSMPLS

TU-LESS: TU-LESS group will receive TU-LESS for myomectomy; MPLS group will receive MPLS for myomectomy

MPLS: Patients with uterine who plan to receive MPLS for myomectomy

Study summary

Myomectomy was preferably applied in females with reproductive requirements, which could be achieved by transumbilical laparoendoscopic single-site surgery (TU-LESS) or multi-port laparoscopic surgery (MPLS). Power morcellation used in MPLS was correlated with unidentified risk of tumor dissemination, especially in cases with accidental surgical findings of uterine sarcoma or leiomyosarcoma. Moreover, TU-LESS was reported to exceed MPLS in fast recovery. Therefore, the aim of this prospective cohort study is to compare the effectiveness of fast recovery and relative risk of tumor dissemination between TU-LESS and MPLS in myomectomy for the treatment of uterine fibroids.

Eligibility

Sex
FEMALE
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * diagnosed with uterine fibroids before surgery on the basis of radiological or other examinations * will consider TU-LESS or MPLS for myomectomy Exclusion Criteria: * patients reluctant to long-term follow-up

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
West China Second University Hospital Chengdu Sichuan

More West China Second University Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06244251 on ClinicalTrials.gov ↗ ← All trials in China