Skip to content

A randomized controlled study of epidermal neuroelectric stimulation combined with accelerated rehabilitation surgery to promote the recovery of intestinal function in patients after gynecological abdominal surgery

A randomized controlled study of epidermal neuroelectric stimulation combined with accelerated rehabilitation surgery to promote the recovery of intestinal function in patients after gynecological abdominal surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045723
Enrollment
Unknown
Registered
2021-04-23
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-12-06

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

Conditions

The intestinal function of the patient was restored after gynecological abdominal surgery

Interventions

Experimental group:ERAS perioperative period treatment and electrophysiological stimulation after surgery
Control group:ERAS perioperative period treatment

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years; 2. Gynaecological benign and malignant diseases with clear indications for surgery; 3. Intended gynecologic laparotomy; 4. ASA class I-II; 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Chronic inflammatory bowel disease, irritable bowel syndrome, history of previous gastrectomy surgery, history of previous abdominal surgery, undergoing treatment that may affect acetylcholine levels; 2. Acute infectious phase, preoperative deep vein thrombosis or hypercoagulable state, fasting blood glucose > 11.1mmol/l, blood pressure > 160 / 100mmhg, liver and kidney dysfunction, mental illness and other surgical contraindications; 3. Contraindication to NSAIDs (peptic ulcer, history of allergy to NSAIDs, asthma on aspirin); 4. Emergency surgery; 5. Wear a pacemaker.

Design outcomes

Primary

MeasureTime frame
Time to restore intestinal function;

Secondary

MeasureTime frame
Incidence of intestinal obstruction after surgery;Gastrointestinal decompression utilization;The first exhaust time after surgery;Bristol stool evaluation scale;Postoperative pain score (2h, 6h, 24h, 48h);Day of hospitalization;Re-hospitalization rate;Hospitalization costs;GIQLI quality of life score;

Countries

China

Contacts

Public ContactLiu Haiyuan

Peking Union Medical College Hospital

liuhaiyuan_pumc@126.com+86 13811580852

Outcome results

None listed

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