Gabapentin on Postoperative Pain Associated With Ureteroscopy and Stents Insertion (NCT03151746) | Clinical Trial Compass
TerminatedPhase 4
Gabapentin on Postoperative Pain Associated With Ureteroscopy and Stents Insertion
Stopped: Insufficient enrollment
United States20 participantsStarted 2018-01-14
Plain-language summary
The study's objective is to determine the efficacy of preoperative gabapentin in relieving postoperative pain, reducing opioid use and improving quality of recovery in subjects undergoing urologic surgery.
Investigators hypothesize that subjects receiving gabapentin will have lower pain scores, less opioid consumption and better quality of recovery as compared to subjects who are given a placebo.
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age 18 years to 75 years
* Patients with obstructive kidney stones undergoing elective ureteroscopy or cystoscopy with Ureteral stent placement
Exclusion Criteria:
* Age less than 18 or more than 75 years
* Acetaminophen allergy
* Gabapentin allergy
* Hydromorphone allergy
* Chronic use of gabapentin
* History of chronic pain (Pain for \> than 3 months)
* Chronic renal insufficiency (Creatinine \> 1.3)
* Seizure disorder
* Psychiatric disorders (medically treated)
* Chronic use of anticonvulsants, antidepressants, antipsychotics (use \> 3 months)
* Antacids ingested within 2 hours prior to surgery
* History of gastric or duodenal ulcer
* Pregnant or lactating
* Inability to communicate in English
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.