Skip to content

Surgical comparison of transvaginal and umbilical single port laparoscopic treatment for benign ovarian cysts: an empirical analysis based on randomized controlled trials

Surgical comparison of transvaginal and umbilical single port laparoscopic treatment for benign ovarian cysts: an empirical analysis based on randomized controlled trials

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082727
Enrollment
Unknown
Registered
2024-04-07
Start date
2024-04-10
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

Benign ovarian cyst

Interventions

TU-LESS group:Using transumbilical single port laparoscopy surgery

Sponsors

Chengdu Women's and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Patients with benign ovarian cysts with a maximum diameter of<10cm and no clever cysts; 2) Indications for laparoscopy; 3) Sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Under 18 years old, over 60 years old; 2) No sexual history; 3) Vaginal stenosis; 4) Vaginitis; 5) Severe pelvic adhesions; 6) Suspected to be malignant; 7) Pregnancy status; 8) Hernia history; 9) History of rectal surgery; 10) Severe internal and external complications that cannot tolerate laparoscopic surgery; 11) History of severe scar on the navel.

Design outcomes

Primary

MeasureTime frame
Baseline information;Surgical success rate;Sexual activity score;Complications during surgery;Postoperative complications;

Secondary

MeasureTime frame
Incision complications;Intraoperative bleeding volume;Duration of surgery;Postoperative pain score;Postoperative intake of painkillers;Hospitalization days;Patient satisfaction;Exhaust time;

Countries

China

Contacts

Public ContactDan Feng

Chengdu Women's and Children's Central Hospital

fengdan11071@163.com+86 134 0850 5176

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026