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Evaluating Artisential Laparoscopic Instruments in Gynecologic Surgery

NCT06050161 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-09-22

No results posted yet for this study

Summary

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

Conditions

  • Pelvic Organ Prolapse
  • Abnormal Uterine Bleeding
  • Mesh Augmentation
  • Laparoscopic Surgery
  • Robotic Surgical Suturing
  • Laparoscopic Hysterectomy
  • Minimally Invasive Surgery

Interventions

DEVICE

Articulating laparoscopic instrument

The Artisential articulating laparoscopic instrument will be evaluated for efficacy and safety in suturing during minimally invasive gynecologic surgery.

DEVICE

Conventional laparoscopic instrument

Conventional laparoscopic instruments will be evaluated for efficacy and safety in suturing during minimally invasive gynecologic surgery.

DEVICE

Robotic surgical instrument

Robotic surgical instruments will be evaluated for efficacy and safety in suturing during minimally invasive gynecologic surgery.

Sponsors & Collaborators

  • Livs Med

    collaborator UNKNOWN

  • Kern Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-20
Primary Completion
2027-09-20
Completion
2027-09-20
FDA Device
Yes

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06050161 on ClinicalTrials.gov