Efficiency & Safety of Water Birth

Clinical Trial Description

Investigators will study medical records of woman who have water birth and evaluate different parameters. Study lasts from February 2020 till April 2021. The questionnaire contain information about woman's expectations of labour Number of participant is approximately 500. ;

Study Design

Related Conditions & MeSH terms

Water Birth

See also
	Status	Clinical Trial	Phase
	Completed	`NCT06429111` - Effectiveness and Safety in Maternal and Neonatal Outcomes in Water Birth.
	Recruiting	`NCT06441370` - Patient Satisfaction During Physiological Water or Land Birth: a Prospective Study in an French Tertiary Maternity Unit.

See also

Status

Clinical Trial

Phase

Completed

NCT06429111 - Effectiveness and Safety in Maternal and Neonatal Outcomes in Water Birth.

Recruiting

NCT06441370 - Patient Satisfaction During Physiological Water or Land Birth: a Prospective Study in an French Tertiary Maternity Unit.

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04239300
Study type	Interventional
Source	Akusherstvo Pro
Contact
Status	Completed
Phase	N/A
Start date	March 11, 2020
Completion date	April 27, 2021

Efficiency and Safety of Water Birth

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms