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Application of Electrophysiological Suitable Technique in Perioperative Rapid Rehabilitation of Urology and Andrology

Application of Electrophysiological Suitable Technique in Perioperative Rapid Rehabilitation of Urology and Andrology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048505
Enrollment
Unknown
Registered
2021-07-09
Start date
2021-07-07
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

Perioperative Rapid Rehabilitation of Urology and Andrology

Interventions

Treatment group:bioelectrical stimulation

Sponsors

Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients in need of surgical treatment for pelvic diseases of urology department admitted nationwide; 2. Aged 18 to 80 years; 3. Signed the informed consent; 4. Valid case data should be collected from no less than 3000 cases.

Exclusion criteria

Exclusion criteria: 1. Patients with major medical diseases who cannot tolerate surgery; 2. Patients with a history of major surgical operations; 3. Patients with severe scar constitution; 4. Patients with severe diabetes, uncontrolled hypertension, and other diseases that seriously affect the rapid postoperative recovery; 5. The treatment site is damaged, ulcerated or infected; 6. Coma, acute infection, pregnancy, menstrual period, uterine massive bleeding; 7. Patients with high fever, heart, liver and renal insufficiency; 8. Upon or near medical stimulators and monitors such as cardiac stents and pacemakers or their leads; 9. Patients with a history of deep venous thrombosis of the lower limbs, malignant tumors or other chronic diseases; 10. Electrical stimulation for contraindications; 11. Anterior cervical region, sinus region, larynx muscles, phrenic nerve or vagus nerve region; 12. Patients who are hesitant or uncooperative; 13. Patients who cannot follow up as requested.

Design outcomes

Primary

MeasureTime frame
perioperative health questionnaire;Mean duration of abdominal incision pain;Abdominal incision healing grade;Intestinal sound recovery time;First exhaust time;The incidence of abdominal pain and distension;time of inurethral catheter;residual urine volume;The incidence of urinary retention;The incidence of chronic pelvic and abdominal pain and anal swelling;The incidence of vulva edema and infection;The healing grade of vulvar incision;Incidence of thrombus;Mean extubation time for pelvic and abdominal drainage;Average hospitalization days;Incision skin temperature;Postoperative gastrointestinal temperature;Postoperative bladder residual urine volume;Postoperative pelvic temperature;Postoperative local body surface temperature of vulva;Body surface temperature of lower limbs;Postoperative temperature of pelvis and peritoneal cavity;Postoperative head surface temperature;

Countries

China

Contacts

Public ContactLiu Xiaming

Second Clinical College, Tongji Medical College, Huazhong University of Science and Technology

xmliu77@hust.edu.cn+86 18627970295

Outcome results

None listed

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