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Cost-Minimization Analysis After a Targeted Intervention for EGD and Colonoscopy

Cost-Minimization Analysis and Its Impact on Resource Utilization After a Targeted Intervention for EGD and Colonoscopy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02328001
Enrollment
969
Registered
2014-12-31
Start date
2014-12-31
Completion date
2015-10-31
Last updated
2017-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Focus of the Study is Cost-minimization Analysis

Brief summary

This study performs a single intervention of informing endoscopists how much the disposable accessories cost following each procedure. Following this single and simple intervention, prospective analysis of EGD and colonoscopy accessory use and pathology specimen costs will be compared to the same resource costs during a control period where endoscopists are blinded to their observation.

Detailed description

This study is a prospective cost-identification and cost-minimization analysis of accessories used during the EGD and colonoscopy procedures. The endoscopists will be the participants under study and not the patients. The study will be conducted in two phases - pre and post-intervention phases. Each phase will include a minimum of 337 combined EGD and colonoscopy procedures and a total of upto a minimum 674 and a maximum of 1200 procedures for both phases. All consecutive patients undergoing EGD and colonoscopy will be included. For the first phase of the study, the endoscopist will not be made aware of the study and also will not be briefed at the end of the procedure with the number of accessories used during the procedure and the dollar value of the accessories. For the second phase of the study, endoscopist will be briefed by the endoscopy nursing staff after completion of each procedure about the total number of accessories used and the dollar value of the accessories used during the procedure. Once the study is completed, endoscopists will be debriefed about the study and outcomes.

Interventions

BEHAVIORALDebriefing endoscopists of the procedure accessory costs

Informing endoscopists of the number of accessories used and the dollar value of the accessories

Sponsors

Sindhu R Kaitha, MD
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults with age of 18 or greater * All races * Indication for therapeutic EGD or colonoscopy * Outpatient procedures done at OU Physicians Building endoscopy unit * Procedure is performed by one of the observed endoscopists

Exclusion criteria

* Pediatric population * Diagnostic EGD and colonoscopy procedures

Design outcomes

Primary

MeasureTime frameDescription
Total cost of accessory use and pathology specimen costsUp to 5 monthsThe cost of accessory and pathology specimens would be assessed immediately post-procedure during phase 2

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026