Not Yet RecruitingNot Applicable

Evaluating Artisential Laparoscopic Instruments in Gynecologic Surgery

50 participantsStarted 2023-09-20

Plain-language summary

This study evaluates the efficacy and safety of Artisential laparoscopic instruments in minimally invasive gynecologic surgery.

Who can participate

Age range22 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient scheduled for robotic or laparoscopic total hysterectomy * Patient scheduled for robotic or laparoscopic sacrocolpopexy Exclusion Criteria: * Not a candidate for the above surgical procedures

What they're measuring

Mesh suturing time

Timeframe: Intraoperative

Vaginal cuff suturing time

Timeframe: Intraoperative

Trial details

NCT IDNCT06050161

SponsorKern Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-09-20

Contact for this trial

Yufan B Chen, MD

661-326-2000 Yufan.Chen@kernmedical.com

View on ClinicalTrials.gov More Pelvic Organ Prolapse trials