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A randomized controlled trial for comparing the single hole laparoscopy with porous laparoscopy in the treatment of myomectomy

A randomized controlled trial for comparing the single hole laparoscopy with porous laparoscopy in the treatment of myomectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017089
Enrollment
Unknown
Registered
2018-07-11
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

diseases of obstetrics and gynecology

Interventions

Group 2:Porous hole laparoscopy

Sponsors

Southwest Hospital affiliated to the Army Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Women aged 18 to 55 years old; (2) Symptomatic uterine fibroids (menstrual change, compression symptoms or infertility); (3) The largest uterine myoma is not more than 12 cm; (4) Without the history of abdominopelvic cavity surgery; (5) The desire for myomectomy of uterine myoma; (6) Agree to participate in the study and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Cannot tolerate the peritoneoscope surgery since the serious internal medicine complication; (2) Women in pregnancy; (3) Subserous myoma and type I submucous myoma with pedicle; (4) History of pelvic abdominal surgery; (5) There are other malignant lesions in the appendage of the uterus; (6) Patients who had received chemotherapy or pelvic radiotherapy in the past; (7) During the active period of reproductive system, urinary system or systemic infection; Coagulant dysfunction or those who are receiving therapeutic anticoagulant drugs; (8) Coagulant dysfunction or those who are receiving therapeutic anticoagulant drugs; (9) Patients with chronic pelvic pain; (10) BMI>30; (11) Researchers believe that other medical or psychological diseases that may exist in the patient, who may not be able to cooperate with the researchers.

Design outcomes

Primary

MeasureTime frame
Operation time;

Secondary

MeasureTime frame
Intraoperative bleeding;Days of hospitalization;

Countries

China

Contacts

Public ContactWang Yanzhou

Southwest Hospital affiliated to the Army Military Medical University

w.y.z@foxmail.com+86 18680893816

Outcome results

None listed

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