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Difference between efficacy of anesthesia in pushing and injection of lidocaine in head, hand and foot wounds

Comparison of the pushing of lidocaine on the wound versus lidocaine injection in anesthesia of the head and limb wounds

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201511097327N6
Enrollment
150
Registered
2016-01-29
Start date
2015-07-23
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

Condition 1: Head skin wound. Condition 2: Upper limb wound. Condition 3: Lower limb wound. Open wound of scalp Open wound of upper limb, level unspecified Open wound of lower limb, level unspecified

Interventions

Intervention 1: Intervention group: 4 milligrams lidocaine per each 5 kilograms of body weight from 2% lidocaine ampul will be pushed on the wound and after 2 minutes suturing will be performed. Int
Treatment - Drugs
Intervention group: 4 milligrams lidocaine per each 5 kilograms of body weight from 2% lidocaine ampul will be pushed on the wound and after 2 minutes suturing will be performed.
Control group: 4 milligrams lidocaine per each 5 kilograms of body weight from 2% lidocaine ampul will be injected in the wound and after 2 minutes suturing will be performed.

Sponsors

Student Research Committee of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients between 18 and 60 year old; wound size less than 3 centimeters. Exclusion criteria: Patients with human or animal bite wounds; wound of ear; wound of thumb or toe; wounds on the joints; usage of corticostroids or anticoagulants or immunosuppresants; patients with big and deep wounds; loss of consciousness ( GCS equal to or less than 14); patients with diabetic neuropathia or sensation disorders.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wound pain severity. Timepoint: Before usage of anesthetics, during the useage of anesthetics, during the suturing ( 2 minutes after the usage of anesthetics ). Method of measurement: Visual analoge score, Severity of the pain in proportion to millimeter from 0 to 100 will be measured.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Samad Shams Vahdati

Tabriz University of Medical Sciences

Shams@tbzmed.ac.ir+98 41 3569 4100

Outcome results

None listed

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