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A randomized controlled study of different bowel preparation program before focused ultrasound ablation surgery for uterine fibroids

A randomized controlled study of different bowel preparation program before focused ultrasound ablation surgery for uterine fibroids

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102284
Enrollment
Unknown
Registered
2025-05-12
Start date
2024-03-14
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Terine fibroid

Interventions

Testl group:Bowel preparation method without cleansing enema
Control group:Routine preoperative bowel preparation

Sponsors

Qingdao Women and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 47 Years

Inclusion criteria

Inclusion criteria: 1. Patients with uterine fibroids suitable for FUAS treatment after preoperative evaluation; 2. No mental illness and voluntary participation in the study.

Exclusion criteria

Exclusion criteria: 1.Inability to take oral laxatives or tolerate enemas; 2.History of chronic constipation; 3.Previous surgical procedures potentially resulting in pelvic adhesions (excluding simple hysteroscopy procedures); 4.Concomitant severe cardiac, hepatic, renal, or other serious diseases.

Design outcomes

Primary

MeasureTime frame
Lesion ablation rate;Whether intestinal injury occurs;Satisfaction with bowel preparation;

Secondary

MeasureTime frame
Surgical field satisfaction;Perioperative incidence of electrolyte disorder;Time to first postoperative flatus;

Countries

China

Contacts

Public ContactYun Tang

Qingdao Women and Children's Hospital

5466042@qq.com+86 185 5326 2758

Outcome results

None listed

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