Trials / Completed
CompletedNCT05705050
Aminophylline Infusion on Pain Intensity After Ureterocopic Lithotripsy
Effect of Intraoperative Aminophylline Infusion on Pain Intensity After Ureterocopic Lithotripsy Surgeries
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Tanta University · Academic / Other
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
This study will be conducted to evaluate the effect of intraoperative systemic aminophylline infusion on pain intensity in patients undergoing ureteroscopic lithotripsy surgeries with ureteric stent placement at the end of the procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aminophylline group | Patients will receive 4 mg/kg aminophylline diluted in 100 ml normal saline over 20 minutes after induction of anesthesia and positioning of patients in lithotomy position. |
| OTHER | Control group | Patients will receive 100 ml normal saline over 20 minutes after induction and lithotomy positioning. |
Timeline
- Start date
- 2023-02-15
- Primary completion
- 2023-06-18
- Completion
- 2023-06-19
- First posted
- 2023-01-30
- Last updated
- 2023-06-27
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT05705050. Inclusion in this directory is not an endorsement.