Oral Misoprostol Versus Vaginal Dinoprostone For Induction Of Labour: A

See also
Status	Clinical Trial	Phase
Completed	`NCT02539199` - Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour	Phase 4
Completed	`NCT04514770` - Impact of Early Versus Late Amniotomy on Labour Induction in Nulliparous Women After Vaginal Misoprostol	N/A
Completed	`NCT03016208` - The Misoprostol Vaginal Insert for Labour Induction	N/A
Completed	`NCT02904317` - Misoprostol for Labour Induction	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT02539199 - Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour

Phase 4

Completed

NCT04514770 - Impact of Early Versus Late Amniotomy on Labour Induction in Nulliparous Women After Vaginal Misoprostol

N/A

Completed

NCT03016208 - The Misoprostol Vaginal Insert for Labour Induction

N/A

Completed

NCT02904317 - Misoprostol for Labour Induction

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	NCT02168881
Study type	Interventional
Source	Ain Shams University
Contact	Marwan Osama Elkady
Phone	+201205533315
Status	Recruiting
Phase	N/A
Start date	May 2014

Oral Misoprostol Versus Vaginal Dinoprostone For Induction Of Labour: A Randomized Controlled Clinical Trial

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms