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Ice effect on pain reduction due to needle insertion during digital block

Clinical trial of comparison of needle stick pain due to digital block in finger traumatic patients with and without using an ice in site of damage.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010731807N1
Enrollment
100
Registered
2017-09-23
Start date
2016-02-19
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

Finger trauma. Disorders of synovium and tendon, Other soft tissue disorders

Interventions

Intervention 1: Case group: There are 50 patients in this group. Injured finger is covered by ice for 6 minutes before needling. Afterwards, finger is anesthetized by 3 milliliters lidocaine. Interven
Treatment - Other
Treatment - Drugs
Case group: There are 50 patients in this group. Injured finger is covered by ice for 6 minutes before needling. Afterwards, finger is anesthetized by 3 milliliters lidocaine.
Control group: There are 50 patients in this group. Finger is anesthetized by using Lidocaine, with no ice application.

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Informed consent (according standard consent), age range: 16-50 years old, fingers trauma which need medical procedures or extra assessment under local anesthesia. Exclusion criteria: Pregnant women, history of reaction to the local anesthetic agents, history of sensitivity to cold, unable to make communication, phobia, opium using during 6 hours before admission, emergent situations, unstable medically patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain due to needle stick of digital block. Timepoint: On admission, after using ice, time of skin needling, during injection. Method of measurement: NRS Questionnaire.

Secondary

MeasureTime frame
Patient satisfaction. Timepoint: At the end of procedure. Method of measurement: Questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Rasooli

Sina Hospital

f-rasooli@tums.ac.ir+98 21 6634 8500

Outcome results

None listed

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