Skip to content

Efficacy Analysis of Sacral Nerve Modulation for Low Anterior Resection Syndrome in Patients with Low Rectal Cancer Undergoing Intraoperative Radiotherapy

Efficacy Analysis of Sacral Nerve Modulation for Low Anterior Resection Syndrome in Patients with Low Rectal Cancer Undergoing Intraoperative Radiotherapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104391
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Low Anterior Resection Syndrome

Interventions

Treatment group:sacral neuromodulation

Sponsors

The Second Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Over 18 years old, gender not limited; (2) Previously diagnosed with rectal cancer, the tumor location was less than 5cm away from the anus, and underwent radical anterior resection of rectal cancer (intraoperative radiotherapy); (3) The LARS score was >=29 points during the 7-day screening period; (4) The anal sphincter was retained during the operation and the continuity of the rectum was intact. (5) Voluntarily participate in this clinical study. Before the start of the study, the subjects sign the written informed consent form. (6) After enrollment, it was agreed not to increase or decrease the related drugs that affect LARS symptoms and pelvic function at will during the trial period; (7) Be able to communicate well with the researcher and be willing to follow the entire trial requirements.

Exclusion criteria

Exclusion criteria: (1) Combined with irritable bowel syndrome, inflammatory bowel disease, active perianal abscess or anal fistula, severe rectal prolapse, and repeated intestinal infections; (2) Those who have received radiotherapy before radical surgery; (3) The time for radical surgery/preventive stoma reduction surgery is less than 12 months; (4) Those who undergo radical surgical resection of intestinal segments other than the rectum; (5) Patients with permanent stoma; (6) Tumor recurrence and metastasis occurred during the follow-up period of the tumor; (7) Pregnant and lactating women; (8) Mental disorders can not cooperate with doctors; (9) There are concomitant diseases that seriously affect health; (10) Other circumstances where the researcher deems it inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Therapeutic efficiency;

Secondary

MeasureTime frame
LARS score;Wexner score;FIQoL Score;Efficacy satisfaction;Bowel diary;

Countries

China

Contacts

Public ContactMin Wang

The Second Hospital of Jilin University

wangmin2009@jlu.edu.cn+86 130 7437 3336

Outcome results

None listed

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