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Comparitive Study Between the effect of Intra techal Petidine and Lidocaine versus Standard Lidocaine on Hemodynamics in Open Prostatic Surgery

Comparitive Study Between the effect of Intra techal Petidine and Lidocaine versus Standard Lidocaine on Hemodynamics in Open Prostatic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903061936N2
Enrollment
78
Registered
2010-10-15
Start date
2009-12-08
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

To study effect of intratechal standard lidocaine and mixture of lidocaine and pethidine on hemodynamic of patient in open prostatectomy. -

Interventions

Intervention 1: In control group all patient received lidocaine 5% intratechally (2 cc)and needle entrance is space L4-L5.Other intervention in two group is same. Intervention 2: In case group all pat
Prevention
In control group all patient received lidocaine 5% intratechally (2 cc)and needle entrance is space L4-L5.Other intervention in two group is same.
In case group all patient received lidocaine 5% pulse pethidine 0/5 mg/kg up to 2 cc intratechally and needle entrance is space L4-L5.Other intervention in two group is same.

Sponsors

Research committee of medical science of bushehr university
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: All patient who are candidates for open prostatectomy are eligible to participate in the study. Exclusion criteria: age above 75 and below 45, history of sensitivity to opioid, unwilling to participate and coagulopathy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemodynamic change (BP change). Timepoint: pre induction and in minute 1,2,3,5,10,15,20,25,30,45,60,90,120. Method of measurement: NIBP monitoring.

Secondary

MeasureTime frame
Temperature change. Timepoint: 60 minute. Method of measurement: Temperature Monitoring.;Post operative nausea and vomiting. Timepoint: 120 minute. Method of measurement: observation.;Post operative pain. Timepoint: 120 minute. Method of measurement: Analogous pain score.;Intra operative blood loss. Timepoint: 120 minute. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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