A Clinical Study for the Effect of Shenbing Prescription on Gastrointestinal Function after Gynecological Abdominal Surgery

Not Applicable

• Conditions: Gynecological patients after abdominal surgery

• Registration Number: ITMCTR1900002272
• Lead Sponsor: Guangdong Provincial Hospital of Chinese Mediciine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1) Patients after gynecological laparoscopy and laparotomy.
2) 40 -70 years old.
3) The operation time is 1-4 hours.
4) anesthesia time 1.5-4.5 hours.
5) Traditional Chinese medicine syndrome is characterized by qi deficiency and qi stagnation, and obstruction of fu-organs and qi.
6) Those who have signed the informed consent form.

Exclusion Criteria

1) Malignant tumor requires extended radical surgery/enterostomy or advanced malignant fluid and extreme debility.
2) Patients with heart, liver, kidney, brain, diabetes, hypertension and other complicated diseases that cannot be controlled after treatment and have obvious symptoms.
3) Persons with mental diseases, allergy to therapeutic drugs, pregnant women or breast-feeding.
4) serum albumin < 27g/l in patients with moderate or above malnutrition; Or prealbumin < 0.14g/l.
5) Severe intestinal adhesion after another abdominal operation.
6) If the intraoperative blood loss exceeds 400ml, or if blood transfusion is needed.
7) Severe Complication (medicine) occurred within 6 hours after operation.
8) Postoperative intraperitoneal thermal perfusion is required.
9) Drugs or therapies that have obvious effects on gastrointestinal function must be used after operation.
10) Patients currently participating in or having participated in other clinical trials within 1 month before this study.
11) Researchers think it is inappropriate to conduct this clinical research.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Brain gut peptide hormone 3 items;Time of first anal exhaust and defecation after operation;