Skip to content

The Evaluation of Effect of Addition of Different Doses of Verapamil to 1.5% Lidocaine on Sensory and Motor Axillary Block

The Evaluation of Effect of Addition of Different Doses of Verapamil to 1.5% Lidocaine on Sensory and Motor Axillary Block

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903094050N1
Enrollment
92
Registered
2010-06-13
Start date
2008-10-22
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

regional anesthesia.

Interventions

Group B, The patients will receive Verapamil 5mg plus 34cc lidocaine 1.5%.
Treatment - Drugs
Group A, The patients will receive only 34cc Lidocaine 1.5%
Group C, The patients will receive Verapamil 10 mg plus 34cc Lidocaine 1.5%
Intervention 1: Group A, The patients will receive only 34cc Lidocaine 1.5%. Intervention 2: Group C, The patients will receive Verapamil 10 mg plus 34cc Lidocaine 1.5%. Intervention 3: Group B, The p
Treatment - Other

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: 1) Upper extrimities surgery including: Hand, Wrist & Forearm 2) Age upper than 18 & lower than 45 3) ASA I & II (American Society of Anesthesia 1 & 2 ) 4) Patient's consent to enter the studyEXCLUSION CRITERIA: 1) Underlying diseases (Hypertension, Diabetes mellitus, Liver diseases, Renal diseases, Coagulopathy) 2) Addiction (opioids & Alcohol) 3)Not consent to enter the study 4) Morbid obesity (weight more than 115 kg) 5)Allergy to local anesthetic drugs 6) Peripheral neuropathy 7) Local infection at injection site 8) Pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Evaluation the time of onset & duration of sympathetic block. Timepoint: Interval time: 0,5,10,15,20,30,45,60,75 minutes & every 15 minutes thereafter after blocking. Method of measurement: Sympathetic block: Alcohol test.;Evaluation the time of onset & duration of sensory & motor block. Timepoint: Interval time: 0,5,10,15,20,30,45,60,75 minutes & every 15 minutes thereafterafter blocking. Method of measurement: Sensory block: Pin prick test/ Motor block: Fingers movement.;Evaluation the duration & quality of analgesia. Timepoint: Interval time: 0,5,10,15,20,30,45,60,75 minutes & every 15 minutes thereafter after blocking and for analgesia 2,4,6,12 ,24 houres in recovery and thereafter. Method of measurement: Analgesia: VAS score.

Secondary

MeasureTime frame
Blood pressure (systolic, disatolic). Timepoint: Just before & after & 15, 30, 45, 60 minutes after axillary block & at the end of surgery and in recovery. Method of measurement: Non invasive blood pressuer automatic monitoring.;Mean arterial pressure. Timepoint: Just before & after & 15, 30, 45, 60 minutes after axillary block & at the end of surgery and in recovery. Method of measurement: Non invasive blood pressuer automatic monitoring.;Heart Rate. Timepoint: Just before & after & 15, 30, 45, 60 minutes after axillary block & at the end of surgery and in recovery. Method of measurement: Non invasive blood pressuer & Heart rate automatic monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKambiz Sadegi

Hazrat Rasool Akram Hospital

kamsadegi@yahoo.co.uk; fsadegi@put.ac.ir+98 21 7798 5238

Outcome results

None listed

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