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A Prospective Cohort Study on the Promotion of Postoperative Recovery after Uterine Operation with Astragalus and Gelatin Granules

A Prospective Cohort Study on the Promotion of Postoperative Recovery after Uterine Operation with Astragalus and Gelatin Granules

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000687
Enrollment
Unknown
Registered
2024-11-11
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

post-abortion

Interventions

Non-exposed group:Patients who are not treated with drugs or who are treated only with conventional Western medicine.
Exposed group:Patients treated with Qigetiaojing granule alone or in combination with conventional Western medicine without using other similar Chinese medicine (proprietary Chinese medicine Chinese m

Sponsors

The Third Hospital of Peking University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. For patients after abortion abortion procedures include: 1) pregnancy < 14 weeks require surgical abortion; 2) Pregnancy < 14 weeks drug abortion incomplete clearance surgery; 3) After spontaneous abortion uterine clearing or curettage is required; 2. Aged between 18 and 40; 3. Within 3 months before pregnancy 21 days = menstrual cycle =35 days 4. The informed consent process shall comply with regulations.

Exclusion criteria

Exclusion criteria: 1. Preoperative patients with endocrine diseases associated with hormonal abnormalities; 2. Patients placed with levonorgestrel intrauterine Release System (LNG-IUS) immediately after surgery; 3. Patients with severe cardiovascular liver kidney and hematopoietic system tumors and other primary diseases mental patients.

Design outcomes

Primary

MeasureTime frame
Menstrual relapse rate;Lower abdominal pain disappear time;Incidence of postoperative complications;Change of symptom/sign score after induced abortion;Vaginal bleeding time;Vaginal bleeding cessation rate;Uterine recovery;Endometrial thickness;Time of menstruation;

Countries

China

Contacts

Public ContactRong Li

The Third Hospital of Peking University

wangbearyang@163.com13701085402

Outcome results

None listed

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