Effects of Preoperative Anxiety & Pain Sensitivity in Cases of Endoscopic

Clinical Trial Summary

The objective of this study was to detect whether preoperative anxiety and pain sensitivity had effects on the consumption of anesthetics, time to achieve desired level of sedation, patient and endoscopist satisfaction, and postoperative recovery time and pain in deep sedation.

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05522127` - Restritive and Liberal Fluid Management and Colonoscopy	N/A
Recruiting	`NCT04477694` - The Effect of Diabetes Mellitus in Colonoscopy Under Sedoanalgesia
Not yet recruiting	`NCT03114774` - Effectivity of Bispectral Index Monitoring in Cases of Endoscopic Retrograde Cholangiopancreatography	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT05522127 - Restritive and Liberal Fluid Management and Colonoscopy

N/A

Recruiting

NCT04477694 - The Effect of Diabetes Mellitus in Colonoscopy Under Sedoanalgesia

Not yet recruiting

NCT03114774 - Effectivity of Bispectral Index Monitoring in Cases of Endoscopic Retrograde Cholangiopancreatography

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	NCT03114735
Study type	Observational
Source	Istanbul Medeniyet University
Contact
Status	Not yet recruiting
Phase	N/A
Start date	April 15, 2017
Completion date	June 1, 2017

Effects of Preoperative Anxiety and Pain Sensitivity in Cases of Endoscopic Ultrasonography Received Sedoanalgesia

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms