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Effect of femoral block versus intravenous infusion pump on postoperative pain in patients underwent surgical repair of anterior cruciate ligament

Effect of femoral block versus intravenous infusion pump on postoperative pain in patients underwent surgical repair of anterior cruciate ligament: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201402279014N27
Enrollment
54
Registered
2014-03-09
Start date
2012-07-22
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 at surgical site at inguinal area. Pain localized to other parts of lower abdomen

Interventions

Intervention 1: Femoral block at the inguinal area using Marcaine 25% 10 ml single dose at the end of surgery. Intervention 2: Intravenous infusion pump using morphine 30 mg in 100 ml normal saline wi
Treatment - Drugs
Femoral block at the inguinal area using Marcaine 25% 10 ml single dose at the end of surgery.
Intravenous infusion pump using morphine 30 mg in 100 ml normal saline with the speed of 4 ml/min single dose at the end of surgery.

Sponsors

Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (a) rapture of anterior cruciate ligament; (b) age of 12 to 70 years. Exclusion criteria: (a) sensitivity to local anesthesia; (b) unable to use infusion pump; (c) history of narcotic addiction; (d) chronic liver failure; (e) renal failure; (f) indication of repairing bilateral anterior cruciate ligament; (g) history of previous inguinal surgery; (h) tumor or enlarged inguinal lymph node; (i) femoral nerve neuropathy; (j) infection of the inguinal area.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain at the surgical site. Timepoint: at zero time and then every 4 hours for 24 hours after surgery. Method of measurement: using VAS scale.

Secondary

MeasureTime frame
Patient’s satisfaction. Timepoint: at zero time and at 12 and 24 hours after surgery. Method of measurement: using Likert scale.;Nausea and vomiting. Timepoint: at zero time and then every 4 hours for 24 hours after surgery. Method of measurement: by question.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Navid Hadadzadegan

Beasat Hospital

hadadzadegan1359@yahoo.com00

Outcome results

None listed

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