MedPath

Effect of ketorolac and dexamethasone injections on pain after renal stent surgery

Phase 2
Conditions
Preventing renal colic post stent removal
Urological and Genital Diseases
Registration Number
ISRCTN14221501
Lead Sponsor
Center for Fundamental Biomedical Clinical Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
174
Inclusion Criteria

1. Patients who underwent stent placement for renal/ureteral stones and returned for cystoscopical stent removal
2. Age between 20 and 85 years old
3. Providing informed consent

Exclusion Criteria

1. Absolute or relative contraindication to ketorolac or dexamethasone
2. Acute or chronic renal failure (estimated glomerular filtration rate <50)
3. History of GI bleeding or peptic ulcer disease
4. Elevated risk of bleeding including cerebrovascular bleeding, haemorrhagic diathesis, use of any anticoagulants, or any bleeding disorder
5. Systemic infections or cerebral malaria
6. Use of live or live-attenuated vaccines
6. Concurrent use of NSAIDs or corticosteroids
7. Pregnancy
8. Breastfeeding

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain measured using the visual analogue score (VAS) on day 1 and day 7
Secondary Outcome Measures
NameTimeMethod
1. Opioid use, measured by the number of patients with any opioid use on day 1<br>2. Urgent pain-related clinical encounters, measured by the number of pain-related clinical encounters in the emergency department since the stent removal<br>3. Subjective renal colic symptoms, measured by the number of patients that experienced renal colic symptoms since the stent removal to day 7<br>4. Missed days of work, measured by the number of missed days of work since the stent removal to day 7<br>5. Injection complications, measured as the number of patients with any injection complication since the stent removal to day 7
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