Clinical Trials Directory

Trials / Completed

CompletedNCT03131713

Preoperative Acetaminophen and Carbohydrate Loading

Impact of Preoperative Acetaminophen and Carbohydrate Loading to on Pain and Functional Status in Patients Undergoing Mohs Micrographic Surgery for Non-melanoma Skin Cancers

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
101 (actual)
Sponsor
Tufts Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study's goal is to assess impact of preoperative acetaminophen and oral carbohydrate drinks on pain and functional status experienced by patients undergoing Mohs micrographic surgery for non-melanoma skin cancers. Patients are randomly assigned to receive standard of care or preoperative acetaminophen 1000 mg and Gatorade sports drinks 2 packets before surgery. Patients are then asked to rate their level of pain, anxiety, thirst, hunger, fatigue on a scale of 0-100 on day of surgery before surgery has started, after clearance of skin cancer, and at the end of the visit. Patients are contacted by phone 48 hours after their surgery to assess their maximum level of post-operative pain (rated from 0-100), usage of over the counter or prescribed pain medications, and presence of complications e.g. bleeding, infection, dehiscence. Differences in perioperative functional status and pain medication usage are compared between patients in control and intervention groups.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophenAcetaminophen 1000mg

Timeline

Start date
2016-07-01
Primary completion
2017-12-31
Completion
2017-12-31
First posted
2017-04-27
Last updated
2019-10-07
Results posted
2019-10-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03131713. Inclusion in this directory is not an endorsement.