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Recruiting NCT05205317

Comparison of the Therapeutic Effects of VR and VR + Metformin in the Treatment of Cesarean Section Scar Defect

No phase Interventional Defect

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Metformin Hydrochloride Sustained-release Tablets, Vaginal repair.
Who it may be relevant to
Registry conditions: Defect. Basic parameters: 18 years — 40 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of the Therapeutic Effects of Vaginal Repair and Vaginal Repair + Metformin in the Treatment of Cesarean Section Scar Defect

Overview

Cesarean section scar defect (CSD) is a novel recognized cause of postmenstrual abnormal uterine bleeding in women. No clinical guidelines have been issued for the management of CSD. The investigators have previously demonstrated that vaginal repair of CSD was an relative effective treatment of CSD. However, only 28.2% of the CSD patients normalized to less than 7 days of menstruation, whereas 51.2% of women had 7 to 10 days of menstruation at 6 months post vaginal repair. The previous research suggested that the occurrence of CSD may be related to the aging phenotype of the myometrium. Metformin, as a classic diabetes treatment drug, has an important position in anti-aging therapy. Therefore, the randomized study was designed to evaluate whether the application of metformin in combination with vaginal repair could achieve better clinical effects than those achieved by vaginal CSD repair alone.

Detailed description

The previous research suggested that the occurrence of cesarean section scar defect (CSD) may be related to the aging phenotype of the myometrium. The aging of the myometrium in some cesarean section patients reduces the proliferation and repair of smooth muscle cells and endometrial cells to a certain extent. The prognosis of vaginal repair is poor and the repair of the endometrium during menstruation is not good.

Metformin, as a classic diabetes treatment drug, has an important position in anti-aging therapy. Its research and application range is the widest, and significant results have been achieved in a number of clinical trials. At the same time, its side effects are less than other anti-aging drugs, and the patient adaptability is better. It maybe the best choice for the treatment of anti-aging diseases. Therefore, the randomized study was designed to evaluate whether the application of metformin in combination with vaginal repair could achieve better clinical effects than those achieved by vaginal CSD repair alone.

Interventions

  • Drug Metformin Hydrochloride Sustained-release Tablets
    drug
  • Procedure Vaginal repair
    The procedure of vaginal repair of CSD was shown as following. The bladder was dissected away carefully from the uterus toward the abdominal cavity until the peritoneum was reached. The CSD tissue was cut to the normal healthy muscle after the abdominal cavity had been entered, and the lower uterine segments had been completely exposed. A double layer of 1-0 absorbable interrupted sutures was used to close the incisions.

Primary outcome measures

  • Duration of menstruation (day) [Time frame: 6 months after vaginal repair of CSD]
  • thickness of the remaining muscular layer (TRM) (mm) [Time frame: 6 months after vaginal repair of CSD]
Secondary outcome measures (2)
  • Subsequent pregnancy outcomes [Time frame: At least 1 year after vaginal repair of CSD]
  • Duration of menstruation (day) [Time frame: At least 1 year after vaginal repair of CSD]

Eligibility criteria

Inclusion criteria

  • Patients are younger than 40 and over the age of 18.
  • Clearly diagnosed with CSD.
  • Experiencing clinical features of abnormal uterine bleeding, prolonged menstrual flow (the duration of menstruation is more than 10 days).
  • The thickness of the remaining muscular layer of CSD was less than 3 mm.
  • Normal range of blood sugar and insulin
  • No serious medical problems (important viscera function in the normal range).
  • No uterine fibroids, endometriosis, adenomyosis
  • No malignant tumors.
  • Sign the informed consent.

Exclusion criteria

  • Over the age of 40 or younger than 18;
  • Indefinite diagnosis.
  • Malignant tumors.
  • With severe medical problems (severe liver disease, kidney disease, respiratory diseases, heart disease or uncontrolled diabetes, epilepsy, etc., dysfunction of important organs).
  • Contraindications to metformin (baseline creatinine >124μmol/L, hypersensitivity to metformin, or a metabolic acidosis), use of drugs that might interact with metformin (glyburide, furosemide, or cationic drugs)
  • Pregnant.
  • Mental diseases.
  • Unwilling to comply with the research plan.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine — Shanghai

Identifiers

NCT: NCT05205317 · XH-21-012

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗