Mesalamine for Uncomplicated Diverticular Disease: a Randomized,

Clinical Trial Description

n/a

Study Design

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

See also
Status	Clinical Trial	Phase
Completed	`NCT04310839` - Outpatient Left Laparoscopic Colectomy
Completed	`NCT01488045` - Compare Propofol to Fentanyl and Midazolam for Colonoscopy	N/A
Active, not recruiting	`NCT02591407` - Trial Comparing Transversus Abdominis Plane Block Versus Epidural Anesthesia for Pain Management in Colorectal Surgery	N/A
Active, not recruiting	`NCT01552226` - Compare Preperitoneal Analgesia to Epidural Analgesia for Pain Control After Colon and Rectal Surgery	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT04310839 - Outpatient Left Laparoscopic Colectomy

Completed

NCT01488045 - Compare Propofol to Fentanyl and Midazolam for Colonoscopy

N/A

Active, not recruiting

NCT02591407 - Trial Comparing Transversus Abdominis Plane Block Versus Epidural Anesthesia for Pain Management in Colorectal Surgery

N/A

Active, not recruiting

NCT01552226 - Compare Preperitoneal Analgesia to Epidural Analgesia for Pain Control After Colon and Rectal Surgery

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	NCT01627262
Study type	Interventional
Source	Dr. Falk Pharma GmbH
Contact
Status	Completed
Phase	Phase 2
Start date	May 2002
Completion date	April 2006

Mesalamine for Uncomplicated Diverticular Disease: a Randomized, Double-blind, Placebo-controlled Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms