Immediate Bonding & Caesarean Section

Clinical Trial Summary

The randomised study analyzes the effects of immediate bonding (skin-to-skin contact) on different psychobiological and somatic outcomes of mother and child. The investigators compare 3 bonding conditions. Cortisol and Oxytocin are also measured during the bonding process.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT03176459` - Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-Sections	Phase 4
	Completed	`NCT03834415` - Lactobacillus Reuteri DSM17938 in C-Section Infants	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT03176459 - Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-Sections

Phase 4

Completed

NCT03834415 - Lactobacillus Reuteri DSM17938 in C-Section Infants

N/A

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	NCT02727452
Study type	Interventional
Source	Johann Wolfgang Goethe University Hospital
Contact
Status	Completed
Phase	N/A
Start date	March 2016
Completion date	December 2019

Immediate Bonding and Caesarean Section

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms