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The effect of propofol on transurethral lithotripsy

The effect of propofol on transurethral lithotripsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180606039987N1
Enrollment
158
Registered
2020-04-25
Start date
2018-10-23
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Ureteric stone. Calculus of ureter

Interventions

Intervention 1: Intervention group: All the patients this group will receive 1.5 mg Lidocaine and then 2.5 mg/kg propofol will inject for anesthesia. Intervention 2: Control group: All the patients

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
24 Years to 78 Years

Inclusion criteria

Inclusion criteria: Patients with no history of renal colic, stone passage, history of TUL and anatomical or renal dysfunction, history of pulmonary disease, smoking, substance abuse, corticosteroids, pregnancy Patients must not have allergy to Propofol , egg and soy

Exclusion criteria

Exclusion criteria: All the patients with surgery time more than 2 hours All the patients with intraoperative pressure drop, and use of vasoactive drugs. All the patients with changing of anesthesia method during the surgery All the patients with muscle relaxant injection during surgery All the patients with packed cell transfusion during surgery

Design outcomes

Primary

MeasureTime frame
Percentage of people with ureteral spasm. Timepoint: Measuring the number of spasms in operation. Method of measurement: number.;Anesthesia time. Timepoint: From the beginning of anesthesia to the end of anesthesia. Method of measurement: Minutes.

Secondary

MeasureTime frame
Stone free rate. Timepoint: after surgery. Method of measurement: Imaging evidence.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaleh Ghiasy

Shahid Beheshti University of Medical Sciences

saleh.ghiasy@sbmu.ac.ir+98 21 4442 9976

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026