Skip to content

Investigation of the Results of Single-injection Nerve Block

Comparison of the Results of Single-Injection Nerve Block with the Traditional Method in Patients Requiring Digital Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230410057871N1
Enrollment
80
Registered
2023-07-09
Start date
2023-07-23
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Hand surgery.

Interventions

Intervention 1: Intervention group: The single injection method will be performed by injecting 3 ml of 1% lidocaine at the base of the finger in the proximal volar metacarpophalangeal region. In all c

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients requiring hand surgery at Shohada-ye Ashayer Teaching Hospital in Khorramabad. Age 18 years and older

Exclusion criteria

Exclusion criteria: Subjects with a history of previous surgery on the ipsilateral hand Subjects who discontinue their cooperation with the research team

Design outcomes

Primary

MeasureTime frame
Change in the pain reported by the patient (pain measured by the Visual Analogue Scale). Timepoint: The pain level will be recorded patient at 1, 3, 5, 15, and 20 minutes. Method of measurement: The patient's pain after the injection is measured with a ruler that ranges from 0 to 10 cm so that 0 is the sign of no pain and 10 is the most severe pain ever experienced.

Secondary

MeasureTime frame
Analgesia onset time in patients in the two groups. Timepoint: Minutes 1, 3, 5, 15 and 20. Method of measurement: The level of pain will be recorded at 1, 3, 5, 15, and 20 minutes.;The rate of complications caused by the treatment including arterial blood oxygen saturation below 90% for more than 60 seconds, change in pulse rate or blood pressure (increase or decrease), change in respiratory rate (increase or decrease), side effects (nausea and vomiting or loss of consciousness). Timepoint: Minutes 1, 3, 5, 15 and 20. Method of measurement: Arterial blood oxygen saturation will be measured by a pulse oximeter from the first finger of the right or left hand. Any drop below 90% for more than 60 seconds will be considered positive. Its absolute amount will be recorded in the 5 defined times.;Overall satisfaction of patients 60 minutes after the end of receiving the medication. Timepoint: Minutes 1, 3, 5, 15 and 20. Method of measurement: Overall satisfaction will be evaluated based on a 5-point scale (0=poor, 1=moderate, 2=good, 3=very good, 4=excellent) within 60 minutes after receiving the medication.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArian Karimi Rouzbahani

Khoram-Abad University of Medical Sciences

arian.karimi@sbmu.ac.ir+98 930 675 7977

Outcome results

None listed

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