Ignite Creation Date:
2024-05-06 @ 8:12 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06297720
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-03-07
First Post:
2024-02-05
Brief Title:
Early Oral Hydration After Thoracoscopic Surgery
Sponsor:
Chang Gung Memorial Hospital
Organization:
Chang Gung Memorial Hospital
Study Overview
Official Title:
Safety and Feasibility of Early Oral Hydration After Video-assisted Thoracoscopic Surgery A Prospective Randomized and Controlled Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn about the safety and feasibility of early oral hydration in patients receiving video-assisted thoracoscopic surgery after general anesthesia The main questions aims to answer
the safety and feasibility of oral hydration supplementation in the recovery room following general anesthesia
the degree of improvement in sore throat and dry mouth after oral hydration
the side effects and risks of oral hydration supplementation such as the incidence of postoperative nausea and vomiting
the impact of oral hydration supplementation in the recovery room following general anesthesia on hemodynamics
patient satisfaction with oral hydration supplementation in the recovery room following general anesthesia
Participants will receive a series of oral hydration from swab moistening and ice cube hydration to water hydration in the recovery room Researchers will compare with the standard no-hydration group to see if it is safe and feasible to hydrate patients in the recovery room
the safety and feasibility of oral hydration supplementation in the recovery room following general anesthesia
the degree of improvement in sore throat and dry mouth after oral hydration
the side effects and risks of oral hydration supplementation such as the incidence of postoperative nausea and vomiting
the impact of oral hydration supplementation in the recovery room following general anesthesia on hemodynamics
patient satisfaction with oral hydration supplementation in the recovery room following general anesthesia
Participants will receive a series of oral hydration from swab moistening and ice cube hydration to water hydration in the recovery room Researchers will compare with the standard no-hydration group to see if it is safe and feasible to hydrate patients in the recovery room
Detailed Description:
Anesthesiologists assess the removal of the endotracheal tube post-surgery and the patient is then transferred to the recovery room for rest The principal investigator will evaluate the consciousness status and risk of nausea and vomiting to confirm eligibility for the trial Subsequently the following grouping will be conducted
1 Experimental group
First moisten the patients throat with a cotton swab dipped in water If no nausea or vomiting occurs after five minutes proceed to the next stage
Provide an ice cube for the patient to hold in their mouth If no nausea or vomiting occurs after ten minutes proceed to the next stage
Offer 10-20ml water for the patient to drink under medical supervision If no nausea or vomiting occurs and the patient requests more water administer 10-20ml of water every ten minutes assessing for any adverse effects each time The total water intake should not exceed 500ml
2 Comparison group - standard care without any intervention
Evaluate the level of throat pain using VAS Visual Analogue Scale score the incidence timing frequency of post-operative nausea and vomiting the level of mouth dryness the satisfaction of patients in recovery room and the vital signs
1 Experimental group
First moisten the patients throat with a cotton swab dipped in water If no nausea or vomiting occurs after five minutes proceed to the next stage
Provide an ice cube for the patient to hold in their mouth If no nausea or vomiting occurs after ten minutes proceed to the next stage
Offer 10-20ml water for the patient to drink under medical supervision If no nausea or vomiting occurs and the patient requests more water administer 10-20ml of water every ten minutes assessing for any adverse effects each time The total water intake should not exceed 500ml
2 Comparison group - standard care without any intervention
Evaluate the level of throat pain using VAS Visual Analogue Scale score the incidence timing frequency of post-operative nausea and vomiting the level of mouth dryness the satisfaction of patients in recovery room and the vital signs
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None