CompletedNot Applicable

Study of Laparoendoscopic Single Site Hysterectomy in Benign and Preinvasive Uterine Disease

South Korea424 participantsStarted 2012-11-23

Plain-language summary

To compare the efficacy between single-port and three-port laparoscopic assisted vaginal hysterectomy in patients with benign or preinvasive uterine disease

Who can participate

Age range20 Years – 70 Years

SexFEMALE

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Inclusion criteria

✓. uterine leiomyoma
✓. uterine adenomyosis
✓. Endometrial hyperplasia
✓. cervical intraepithelial neoplasia including carcinoma in situ
✓. Dysfunctional uterine bleeding
✓. Other benign gynecologic disease requiring hysterectomy

What they're measuring

postoperative hospital stay

Timeframe: within 1 week after surgery

Trial details

NCT IDNCT01679548

SponsorAsan Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-12-12

View on ClinicalTrials.gov More Benign or Preinvasive Uterine Disease trials