- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06236074
Comparison of Modified PADSS Between 4 and 24 Hours in Patients Undergoing LC
September 2, 2025 updated by: Niruji Saengsomsuan, Thammasat University Hospital
Comparison of Modified Post-Anesthetic Discharge Scoring System (PADSS) Between 4 and 24 Hours in Patients Undergoing Laparoscopic Cholecystectomy
This study is compare of Modified Post-Anesthetic Discharge Scoring System (PADSS) between 4 and 24 hours in patients undergoing laparoscopic cholecystectomy
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Klongluang
-
Pathum Thani, Klongluang, Thailand, 12120
- Thammasat University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patient undergoing laparoscopic cholecystectomy
- 20-60 years old
- American Society of. Anesthesiologist physical status classification I-III
Exclusion Criteria:
- Turn to open cholecystectomy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Modified Post-Anesthetic Discharge Scoring System (PADSS) between 4 and 24 hours
|
Laparoscopic Cholecystectomy
Observation Modified Post-Anesthetic Discharge Scoring System (PADSS) between 4 and 24 hours
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of Modified Post-Anesthetic Discharge Scoring System (PADSS) Between 4 and 24 Hours in Patients Undergoing Laparoscopic Cholecystectomy
Time Frame: 4 vs 24 hours
|
The modified post-anesthetic discharge scoring system, which consists of five components (each component having 2 points): vital signs, ambulation, nausea or vomiting, pain, and surgical bleeding
|
4 vs 24 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2023
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
April 30, 2025
Study Registration Dates
First Submitted
January 24, 2024
First Submitted That Met QC Criteria
January 31, 2024
First Posted (Actual)
February 1, 2024
Study Record Updates
Last Update Posted (Estimated)
September 9, 2025
Last Update Submitted That Met QC Criteria
September 2, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MTU-EC-AN-1-072/66
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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