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The Effectiveness and Safety of Early Intervention of Sacral Nerve Regulation for Bladder Dysfunction after Radical Cervical Cancer Surgery

The Effectiveness and Safety of Early Intervention of Sacral Nerve Regulation for Bladder Dysfunction after Radical Cervical Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108843
Enrollment
Unknown
Registered
2025-09-08
Start date
2025-09-22
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Cervical cancer

Interventions

Control Group:None
Experimental Group:Sacral Neuromodulation (SNM)

Sponsors

Department of Gynecological Oncology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University, Shanghai 200092, China
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Aged 20 to 80 years; 2. Stage IB1 to IIA1 cervical cancer (FIGO 2018 staging) treated with radical hysterectomy; 3. No indication for postoperative adjuvant chemoradiotherapy based on postoperative pathology; 4. No contraindications to SNM surgery; 5. Good compliance, willing and able to meet trial requirements; 6. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of pelvic radiotherapy; 2. Patients with a history of voiding dysfunction, urinary incontinence, or abnormal preoperative urodynamic findings; 3. Patients in whom lower urinary tract dysfunction due to other causes cannot be ruled out; 4. Patients with severe urinary tract infections or vesicovaginal fistula; 5. Patients with concomitant urinary system tumors, urinary calculi, or other obstructive uropathies; 6. Patients with impaired function of important organs: liver enzymes >2 times the upper limit of normal, creatinine >2 times the upper limit of normal, blood amylase >2 times the upper limit of normal, cardiac function class 3–4, etc; 7. Patients with psychiatric or cognitive impairments who are unable to cooperate with the trial process; 8. Other conditions deemed by the investigator as unsuitable for study participation.

Design outcomes

Primary

MeasureTime frame
The efficacy of urinary improvement at six months postoperatively;

Secondary

MeasureTime frame
Urodynamic parameters;

Countries

China

Contacts

Public ContactXiaoqing Guo

Shanghai First Maternity and Infant Hospital

Xiaoqing_Guo@tongji.edu.cn+86 181 1720 3480

Outcome results

None listed

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