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Perioperative Pregabalin in Ureteroscopy

Perioperative Pregabalin as Part of a Multimodal Treatment Plan for Ureteral Stent Symptoms After Ureteroscopy: a Randomized Controlled Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04122196
Enrollment
118
Registered
2019-10-10
Start date
2020-06-01
Completion date
2024-07-01
Last updated
2025-11-12

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

Conditions

Addiction, Kidney Stone, Opioid Use, Pain, Postoperative

Brief summary

This is a randomized, placebo-controlled, double-blinded study examining the use of perioperative pregabalin in ureteroscopy with stent placement. Ureteroscopy is typically performed for kidney or ureteral stones, but may be performed for other reasons such as for the diagnosis and possible treatment of certain kinds of cancers. As part of the same surgery, a ureteral stent is often placed. The surgery and the stent can cause discomfort, and patients may receive narcotic pain medicine. In other surgeries, a single dose of pregabalin, around one hour before surgery has been shown to decrease the need for pain medication after the surgery. This work will test whether this is true in ureteroscopy by giving eligible patients who agree to participate either pregabalin or a placebo shortly before surgery then examining how much pain medication they use after surgery. A placebo is an inactive medication. Neither the study participant nor the study staff will know who received pregabalin and who received placebo until after the study is over. For completing surveys, patients will receive compensation for their time in the form of gift certificates.

Detailed description

The prevalence of urolithiasis is greater than 8% and increasing in the United States. For those who require surgery, ureteroscopic treatment is common, representing \>120,000 procedures yearly in the United States. This does not include ureteroscopy for other, including diagnosis of structural anomaly and diagnosis and management of ureteral and renal pelvic tumors. Frequently, a ureteral stent is placed intraoperatively. There is post-operative pain in around 80% of patients, and 12% of those undergoing ureteroscopy will have an emergency department visit in the first 30 post-operative days, typically for stent related symptoms or post procedural pain. Aside from the short-term repercussions of ureteroscopy with stent placement there are long-term issues related to pain and the treatment thereof. Recent evidence suggests that approximately 6% of opioid naïve patients who undergo ureteroscopy will become new persistent opioid users. A single perioperative dose of pregabalin has been shown in many surgical contexts to have analgesic, anxiolytic, and opioid sparing effects. A common regimen employed in the literature is a single preoperative dose of 300mg PO pregabalin 1hr before induction of anesthesia. Pregabalin is a well-tolerated gabapentinoid medication with temporary cognition/coordination changes being the most common side effects. There is currently no standard of care for the use of perioperative gabapentinoid medication in ureteroscopy. A pilot was performed looking at such use that demonstrated the safety of this use and the feasibility of studying this at our institution. In this work, the efficacy and safety of perioperative pregabalin in ureteroscopy with stent placement will be evaluated by executing a prospective, double blind, randomized, placebo-controlled trial for the use of perioperative pregabalin in the management of post-ureteroscopy symptoms, with the hypothesis that this treatment is safe and efficacious. Emphasis will be placed on patient-centered outcomes, especially those related to opioid sparing effects, mainly within the first 30 days after the surgery and extending out to one year. The study will be powered with an 80% probability to detect a 10% difference in the primary outcomes. It will also assume a loss to follow up rate of 50%. This will require approximately 200 total subjects with a planned 1:1 placebo to active treatment enrollment ratio. The necessary enrollment can be accomplished in 11 months, allowing for 30 days of follow up within the funding period. The final goal of this project will be at least one paper in a top urology journal. This will contribute to the literature by helping to inform urologists and anesthesiologists on the efficacy and safety of perioperative pregabalin for ureteroscopy with stent placement and will provide data regarding opioid sparing management after ureteroscopy. Opioid related issues abound nationwide and are evident in Missouri. This study has the potential to influence opioid use both in this state and nationwide as it relates to this frequently performed procedure.

Interventions

Patient will receive a compounded version of 300mg pregabalin PO approximately one hour before surgery.

DRUGPlacebo oral tablet

Patient will receive a compounded version of inactive placebo PO approximately one hour before surgery.

Sponsors

University of Missouri-Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

Subject Inclusion: * Age \>= 18 years * Subject Population Undergoing elective ureteroscopy with stent placement at University of Missouri Hospital and affiliated facilities Subject Exclusion: * Renal insufficiency (eGFR \< 60 mL/minute/1.73 m2) * Chronic indwelling ureteral stent (\>30 days in the previous year) * Chronic opioid use * History of opioid abuse * Chronic gabapentinoid use * History of gabapentinoid abuse * Plan for inpatient hospitalization * Pregnancy * Inability of the patient to consent for themselves in English * Allergy to gabapentinoid * Liver failure or hepatic dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale of Pain Score1 hour after arrival to post anesthesia care unitThis was a visual analogue scale of pain as described in Ahles et al 1984. The patients were given a paper with a 10cm horizontal line on it. On the left was marked No pain and on the right Worst pain imaginable. The patients were then asked to mark a vertical line along the 10cm line that indicated where their pain was. The score is the number of centimeters from the left. 0 is minimum (best). 10 maximum (worst).

Secondary

MeasureTime frameDescription
Oral Morphine Equivalents of Opioids PrescribedWithin the first 30 days post-operation
Proportion of Patients With Narcotic PrescriptionWithin the first 30 days post-operation
Number of Unplanned Healthcare InteractionsWithin the first 30 days post-operationUnplanned healthcare interactions include unplanned visits, emergency room visits, admissions to the hospital, and phone calls
Number of Serious Adverse EventsWithin the first 30 days post-operationComposite of unplanned serious adverse events including intensive care unit stay and death
Watson Clock Drawing Test Score1 hour after arrival to post anesthesia care unitThis score is based on the scoring method described in Watson et al 1993. Higher scores demonstrate more errors. A clock is drawn. This is divided into quadrants. For errors in quadrants 1-3 (clock 12-8), a score of 1 is assigned. For errors in quadrant 4, a score of 4 is assigned. The scores are summed. Total scores range from 0 to 7 with 7 representing significant impairment (worst) and 0 representing no impairment (best).

Other

MeasureTime frame
In-facility Oral Morphine EquivalentsDay of surgery
Nausea/Vomiting in PACUIn post anesthesia care unit (usually approximately 1 hour post op)

Countries

United States

Participant flow

Participants by arm

ArmCount
Pregabalin 300mg
Patient will receive a compounded version of 300mg pregabalin PO approximately one hour before surgery. Pregabalin 300mg: Patient will receive a compounded version of 300mg pregabalin PO approximately one hour before surgery.
59
Placebo
Patient will receive a compounded version of inactive placebo PO approximately one hour before surgery. Placebo oral tablet: Patient will receive a compounded version of inactive placebo PO approximately one hour before surgery.
59
Total118

Baseline characteristics

CharacteristicTotalPregabalin 300mgPlacebo
Age, Continuous49 years44 years57 years
First ureteroscopy94 Participants48 Participants46 Participants
In-facility belladonna-opium suppository25 Participants14 Participants11 Participants
In-facility non-steroidal anti-inflammatory drug70 Participants35 Participants35 Participants
Laterality
Bilateral
11 Participants5 Participants6 Participants
Laterality
Left
62 Participants32 Participants30 Participants
Laterality
Right
44 Participants22 Participants22 Participants
Preoperative alpha blocker55 Participants27 Participants28 Participants
Preoperative visual analogue scale of pain0.6 units on a scale0.6 units on a scale0.5 units on a scale
Preoperative Watson Clock Test Score2 units on a scale2 units on a scale2 units on a scale
Prestented38 Participants23 Participants15 Participants
Procedure length38 minutes37 minutes38 minutes
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United States
118 participants59 participants59 participants
Sex: Female, Male
Female
67 Participants36 Participants31 Participants
Sex: Female, Male
Male
51 Participants23 Participants28 Participants
Sheath66 Participants35 Participants31 Participants
Stented at ureteroscopy93 Participants45 Participants48 Participants
Stone location
None
10 Participants3 Participants7 Participants
Stone location
Renal
31 Participants18 Participants13 Participants
Stone location
Ureteral
77 Participants38 Participants39 Participants
Total oral morphine equivalents in 30 days prior4 mg8 mg0 mg

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 590 / 59
other
Total, other adverse events
0 / 590 / 59
serious
Total, serious adverse events
0 / 590 / 59

Outcome results

Primary

Visual Analog Scale of Pain Score

This was a visual analogue scale of pain as described in Ahles et al 1984. The patients were given a paper with a 10cm horizontal line on it. On the left was marked No pain and on the right Worst pain imaginable. The patients were then asked to mark a vertical line along the 10cm line that indicated where their pain was. The score is the number of centimeters from the left. 0 is minimum (best). 10 maximum (worst).

Time frame: 1 hour after arrival to post anesthesia care unit

ArmMeasureValue (MEDIAN)
Pregabalin 300mgVisual Analog Scale of Pain Score3.7 units on a scale
PlaceboVisual Analog Scale of Pain Score2.0 units on a scale
Secondary

Number of Serious Adverse Events

Composite of unplanned serious adverse events including intensive care unit stay and death

Time frame: Within the first 30 days post-operation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pregabalin 300mgNumber of Serious Adverse Events0 Participants
PlaceboNumber of Serious Adverse Events0 Participants
Secondary

Number of Unplanned Healthcare Interactions

Unplanned healthcare interactions include unplanned visits, emergency room visits, admissions to the hospital, and phone calls

Time frame: Within the first 30 days post-operation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pregabalin 300mgNumber of Unplanned Healthcare Interactions8 Participants
PlaceboNumber of Unplanned Healthcare Interactions16 Participants
Secondary

Oral Morphine Equivalents of Opioids Prescribed

Time frame: Within the first 30 days post-operation

ArmMeasureValue (MEDIAN)
Pregabalin 300mgOral Morphine Equivalents of Opioids Prescribed60 mg
PlaceboOral Morphine Equivalents of Opioids Prescribed50 mg
Secondary

Proportion of Patients With Narcotic Prescription

Time frame: Within the first 30 days post-operation

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pregabalin 300mgProportion of Patients With Narcotic Prescription44 Participants
PlaceboProportion of Patients With Narcotic Prescription35 Participants
Secondary

Watson Clock Drawing Test Score

This score is based on the scoring method described in Watson et al 1993. Higher scores demonstrate more errors. A clock is drawn. This is divided into quadrants. For errors in quadrants 1-3 (clock 12-8), a score of 1 is assigned. For errors in quadrant 4, a score of 4 is assigned. The scores are summed. Total scores range from 0 to 7 with 7 representing significant impairment (worst) and 0 representing no impairment (best).

Time frame: 1 hour after arrival to post anesthesia care unit

ArmMeasureValue (MEAN)Dispersion
Pregabalin 300mgWatson Clock Drawing Test Score1.8 units on a scaleStandard Deviation 2.1
PlaceboWatson Clock Drawing Test Score1.8 units on a scaleStandard Deviation 2.2
Other Pre-specified

In-facility Oral Morphine Equivalents

Time frame: Day of surgery

ArmMeasureValue (MEDIAN)
Pregabalin 300mgIn-facility Oral Morphine Equivalents38 mg
PlaceboIn-facility Oral Morphine Equivalents35 mg
Other Pre-specified

Nausea/Vomiting in PACU

Time frame: In post anesthesia care unit (usually approximately 1 hour post op)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Pregabalin 300mgNausea/Vomiting in PACU2 Participants
PlaceboNausea/Vomiting in PACU0 Participants

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