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Comparison of two types of block for analgesia after knee surgery

Femoral nerve block at the adductor canal entrance interventional performance and compare it with the classical method for analgesia after knee surgery in patients who have elective knee surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014111219924N1
Enrollment
96
Registered
2015-01-07
Start date
2012-01-21
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

Local anesthesia. Local anaesthetics

Interventions

Intervention 1: Intervention conducted in the intervention group: Femoral nerve block via adductor canal with the aid of ultrasounography, Once injection,Marcaine 0.125% 10 cc. Intervention 2: Interve
Treatment - Drugs
Intervention conducted in the intervention group: Femoral nerve block via adductor canal with the aid of ultrasounography, Once injection,Marcaine 0.125% 10 cc.
Intervention conducted In control group: Femoral nerve block in inguinal canal with the aid of ultrasounography, Once injection. Marcaine 0.125% 20 cc.

Sponsors

Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 70 Years

Inclusion criteria

Inclusion criteria: The inclusion main criteria: The absence af coagulopathy; ASA 1-2; Elective knee surgery; Age 15-70 y; The absence of opium addiction; The absence of neuropathy; BMI less than 35. The exclusion main criteria: Lack of consent; Creates block side effects.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Analgesia after femoral block or Obturator block. Timepoint: Immediately after blocking and 3, 6, 12 and 24 hours later. Method of measurement: Questionnaire and Examination of patient.

Secondary

MeasureTime frame
Immobility after femoral block or Obturator block. Timepoint: Immediately after blocking and 3, 6, 12 and 24 hours later. Method of measurement: Questionnaire and Examination of patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArmaghan Abbasi Baharanchi

Iran University of Medical Sciences

abbasi.arm8@gmail.com; sh_abbasi23@yahoo.com+98 936 687 9814

Outcome results

None listed

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