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The effect of Ropivacaine on post-operative pain after Transcataneous Percataneous Nepholytotomy

The effect of Ropivacaine on post-operative pain after Transcataneous Percataneous Nepholytotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201307153773N8
Enrollment
60
Registered
2015-01-15
Start date
2013-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pain after Percutaneous Nephrolithotomy. Calculus of kidney

Interventions

Intervention 1: At the end of the operation, patients of intervention group, 30 mL of 0. 2% ropivacaine will be instilled into the renal puncture site, nephrostomy tract, and skin. Postoperatively, pa
Treatment - Drugs
At the end of the operation, patients of intervention group, 30 mL of 0. 2% ropivacaine will be instilled into the renal puncture site, nephrostomy tract, and skin. Postoperatively, patients received
At the end of the operation, patients of control group, 30 mL of saline will be instilled into the renal puncture site, nephrostomy tract, and skin. Postoperatively, patients received Apotel I.V. (Ace

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age:15-60 y; Weight less than 40kg; Percataneous Nepholytotomy operation. Exclusion criteria: Too many kidney stones which Ropivacaine administration reaches over dosage; Retained Kidney stone after operation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 4 and 6 h after operation. Method of measurement: VAS (Visual analogue scale).;Peak End Expiratory Flow Rate. Timepoint: Before operation/6&4 hour after operation. Method of measurement: Blowing at Peak Flow Meter.

Secondary

MeasureTime frame
Peak expiratory flow rate. Timepoint: 4 & 6 h after operation. Method of measurement: Ambulatory PEFmeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarsad Imani M.D.

Tehran University of Medical Sciences

imanifar@tums.ac.ir+98 21 63120

Outcome results

None listed

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