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Clinical Efficacy of Conservative Treatment in Female Patients With Plevic Congestion Syndrome

I

Interregional Clinical Diagnostic Center, Russia

Status

Completed

Conditions

Pelvic Congestion Syndrome

Treatments

Drug: Daflon

Study type

Observational

Funder types

Other

Identifiers

NCT04512443
Daflon25122019

Details and patient eligibility

About

The article presents the results of a randomized, placebo-controlled study of the conservative treatment with Daflon (Detralex) in female patients with Pelvic congestion syndrome .

Enrollment

83 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

•The presence of pelvic varicose veins verified by transvaginal and transabdominal duplex ultrasound scanning

Exclusion criteria

  • Severe disease of the gastrointestinal tract or hematopoietic system
  • Terminal stage of cardiovascular, respiratory, renal or hepatic failure
  • Grade IV malignancy
  • Peripheral artery disease (PAD) of the lower extremities, any type of diabetes, or mental disease.
  • Pregnant women at any gestational age, women who gave birth less than 12 months ago, and breastfeeding mothers.

Trial design

83 participants in 2 patient groups

1
Description:
42 women (treated with Daflon 1000 mg (study group))
Treatment:
Drug: Daflon
2
Description:
41 women (placebo (control group))

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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