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OpenTrials
Completed

NCT Number: NCT03907267

Taurine in Peripartum Cardiomyopathy

Taurine as an adjunct for early left ventricular recovery in peripartum cardiomyopathy

Completed

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Ain Shams University Maternity Hospital

Cairo, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Peripartum Cardiomyopathy

Exclusion criteria

  • Other identifiable cause for heart failure
  • low LVEF ≤ 25%
  • sepsis
  • autoimmune disease
  • severe chronic disease
  • malignancy

Treatment and study plan

Taurine Solution

Drug

Taurine Solution

Normal saline

Dietary Supplement

Normal Saline

Primary outcomes

  1. improvement of the left ventricular ejection fraction >10 %

    Time frame: 1 week

    improvement of the left ventricular ejection fraction >10 %

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Taurine for Early Left Ventricular Recovery in Peripartum Cardiomyopathy

Important dates

Study start
2015
Primary completion
2019
Study completion
2020
First posted
Apr 8, 2019
Registry last updated
Jan 28, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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