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Clinical study for accurate exercise and flora intervention in the treatment of recurrent abortion complicated with metabolic syndrome

Clinical study for accurate exercise and flora intervention in the treatment of recurrent abortion complicated with metabolic syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026336
Enrollment
Unknown
Registered
2019-09-30
Start date
2019-09-23
Completion date
Unknown
Last updated
2020-06-22

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

Conditions

Recurrent spontaneous abortion complicated with metabolic syndrome

Interventions

1:Transportation intervention
2:Flora intervention
3:Exercise and bacterial population intervention
4:no intervention

Sponsors

Shenzhen Maternity and Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) patients in accordance with the RSA diagnostic criteria and combined with MS; (2) patients with a course of at least 6 months; (3) women with an insufficient amount of exercise in the range of 20 to 40 years old; (4) patients with stable disease control in one year without an acute metabolic disorder; (5) the subject is willing to adhere to regular exercise and flora intervention treatment; (6) subject informed consent, and sign the relevant documents. The process of obtaining the informed consent form shall be in accordance with the requirements of the gcp.

Exclusion criteria

Exclusion criteria: (1) Patients with severe myocardial ischemia, proliferative retinopathy, renal insufficiency, malignant hypertension, unstable blood glucose control, and the like; (2) Replacing oral hypoglycemic agents, reducing drugs or regulating blood lipid drugs over the last two months; (3) The body weight was changed by 5% in the past two months; the blood myography was 2.26 mg/ dL (200 µmol/ L); the proteinuria was more than 1 g/ d; the blood pressure was more than 160/95 mm Hg; (4) Other ECG, routine, ophthalmological, blood pressure, etc. were examined for movement contraindication; (5) The abnormal structure of the uterus: such as the uterine malformation; (6) The administration of antibiotics in the last three months; (7) The habit of regulating the intestinal products such as probiotics and biotics.

Design outcomes

Primary

MeasureTime frame
sugar tolerance;insulin;blood fat;glycosylated hemoglobin;interleukin;tumor necrosis factor;Hemorheology;C reactive protein;Analysis of intestinal flora diversity based on 16s rDNA;

Countries

China

Contacts

Public ContactLiu Qingzhi

Department of Reproductive and Immunologic, Shenzhen Maternity and Child Healthcare Hospital

liuqingzhi1002@126.com+86 13825266991

Outcome results

None listed

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