The analgesic effect of paracetamol when added to lidocaine for intravenous regional anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20141121020020N3

Enrollment

Registered

2019-08-18

Start date

2013-07-23

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

Intera venous Regional Anesthesia. Local anaesthetics

Interventions

Intervention 1: Intervention group: All patients would received the same premedication (200 ml of normal saline, 1 mg of midazolam and 50 micrograms fentanyl).intravenous regional anesthesia with 200

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 20--60 years old Patients undergoing hand surgeries ASA ClassI,II

Exclusion criteria

Exclusion criteria: History of allergic reaction Addiction Pregnancy

Design outcomes

Primary

Measure	Time frame
Surgical site pain. Timepoint: After the start of surgical process (at 5, 10, 15, 20, 30, 40 and 50 min) and after the end of surgery. Method of measurement: Visual Analogue Scale (VAS).;Onset and duration of sensory and motor block. Timepoint: From the start of anesthetics injection to the end of operation. Method of measurement: Evaluate the patients response to needle hitting on surgical site and request of the patients to hand flexion and extension.;Time to the first request for analgesic. Timepoint: Once at the moment of first request. Method of measurement: Time elapsed from tourniquet deflation in minutes.	—

Measure

Time frame

Surgical site pain. Timepoint: After the start of surgical process (at 5, 10, 15, 20, 30, 40 and 50 min) and after the end of surgery. Method of measurement: Visual Analogue Scale (VAS).;Onset and duration of sensory and motor block. Timepoint: From the start of anesthetics injection to the end of operation. Method of measurement: Evaluate the patients response to needle hitting on surgical site and request of the patients to hand flexion and extension.;Time to the first request for analgesic. Timepoint: Once at the moment of first request. Method of measurement: Time elapsed from tourniquet deflation in minutes.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahram Seyfi

Babol University of Medical Sciences

ficu_ss@yahoo.com+98 11 3223 8301

Outcome results

None listed

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