Effect of intraincisional bupivacaine infusion in intertrochanteric fracture

Comparison of the effect of continuous infusion of bupivacaine through intra-incisional catheter with control group for postoperative pain relieve in patients with intertrochanteric fracture

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20100127003213N8

Enrollment

Registered

2020-03-16

Start date

2019-03-21

Completion date

Unknown

Last updated

2020-03-24

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

Conditions

Femur fracture. Intertrochanteric fracture of femur

Interventions

Intervention 1: Interventions group 1:At the end of the surgery an intra-incisional catheter (Infiltralong 600, PAJUNK, Geisingen, Germany) will be placed subfascially which will be connected to a 100

Eligibility

Sex/Gender

All

Age

50 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who scheduled to undergo hip nailing surgery and can tolerate surgery under spinal anesthesia American Society of Anesthesiologists (ASA) I-II 50-85 years of age

Exclusion criteria

Exclusion criteria: Uncontrolled seizure Local infection Coagulopathy Thrombocytopenia History of hepatic and renal function impairment narcotic addiction Allergy to drugs which are going to be used in this study History of Psychosomatic pain Psychiatric diseases Diabetic neuropathy 2nd and 3rd degree A-V block

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: Every 15 minutes after surgery (15, 30, 45, 60 minutes) in recovery room, and every 2 hours after transfer to ward . Method of measurement: Numerical Rating Scale of pain.;Total morphine administration. Timepoint: total dose during the first postoperative 24 hours. Method of measurement: dose summation reported in milligrams.	—

Secondary

Measure	Time frame
Patient’s global satisfaction. Timepoint: Discharge from the ward. Method of measurement: ?A 5-point Likert scale: completely satisfied (= 5), partially satisfied (= 4), neutral (= 3), partially dissatisfied (= 2) and completely dissatisfied (= 1).;Ease of ambulation. Timepoint: During admission. Method of measurement: Cumulated Ambulation Score.;Time to first request for analgesia. Timepoint: Time to first request, measured from termination of the procedure and recovery room entry. Method of measurement: minute.;Drug side effects (nausea & vomiting, respiratory depression, urinary retention, drowsiness, pruritus, hypotension, tinnitus). Timepoint: Every four hours for 24 hours. Method of measurement: Occurrence frequency.	—

Measure

Time frame

Patient’s global satisfaction. Timepoint: Discharge from the ward. Method of measurement: ?A 5-point Likert scale: completely satisfied (= 5), partially satisfied (= 4), neutral (= 3), partially dissatisfied (= 2) and completely dissatisfied (= 1).;Ease of ambulation. Timepoint: During admission. Method of measurement: Cumulated Ambulation Score.;Time to first request for analgesia. Timepoint: Time to first request, measured from termination of the procedure and recovery room entry. Method of measurement: minute.;Drug side effects (nausea & vomiting, respiratory depression, urinary retention, drowsiness, pruritus, hypotension, tinnitus). Timepoint: Every four hours for 24 hours. Method of measurement: Occurrence frequency.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSanaz Abbasi

Shiraz University of Medical Sciences

sanaz_med65@yahoo.com+98 71 3647 4270

Outcome results

None listed

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