Continuous Labor Epidural Catheter for Tubal Ligation Study

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05688943` - Comparative Analysis of Spinal Anesthesia Versus General Anesthesia for vNOTES	N/A
Enrolling by invitation	`NCT04757922` - Stop Ovarian Cancer Young; Effect of the Opportunistic Salpingectomy on Age of Menopause
Completed	`NCT00849173` - Global Study of Women's Health
Terminated	`NCT04663568` - Levonorgestrel-releasing Intrauterine System and Tubal Ligation	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT05688943 - Comparative Analysis of Spinal Anesthesia Versus General Anesthesia for vNOTES

N/A

Enrolling by invitation

NCT04757922 - Stop Ovarian Cancer Young; Effect of the Opportunistic Salpingectomy on Age of Menopause

Completed

NCT00849173 - Global Study of Women's Health

Terminated

NCT04663568 - Levonorgestrel-releasing Intrauterine System and Tubal Ligation

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	NCT00898443
Study type	Interventional
Source	University of Alabama at Birmingham
Contact
Status	Terminated
Phase	N/A
Start date	October 2008
Completion date	August 2010

Continuous Labor Epidural Catheter for Tubal Ligation Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms