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Comparison of two ways of analgesia, heamatoma Block and general anesthesia distal radius fractures in patients over than 60 year

Comparison of Heamatoma Block versus general anesthesia in pain control of distal radius fractures in patients over than 60 year

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201608199857N3
Enrollment
68
Registered
2016-09-08
Start date
2016-07-22
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

distal radius fracture. Fracture at wrist and hand level

Interventions

Intervention 1: In intervention group: Hematoma block with Lidocain 2% will be used to analgesia. Intervention 2: In control group: General anesthesia will be used.
Treatment - Drugs
In intervention group: Hematoma block with Lidocain 2% will be used to analgesia
In control group: General anesthesia will be used

Sponsors

Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: isolate displaced distal radius fracture;absence of trauma in other regions; absence of deformity and previous fracture in distal radius,;the age of over 60 Exclusion Criteria: Patients with lung disease;Smoking;coagulopathy; addicted and alcoholic people

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Every 6 hours until discharge. Method of measurement: VAS scoring.

Secondary

MeasureTime frame
Time of hospitalization. Timepoint: Daily. Method of measurement: Days of hospitalization.;Needs to analgesic. Timepoint: Every 6 hours until discharge from hospital. Method of measurement: Dose of consumption.;Infection. Timepoint: Per day until removal of implants. Method of measurement: Clinical examinaton.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Tabrizi

Urmia University of Medical Sciences

Ali.tab.ms@gmail.com+98 44 3345 7286

Outcome results

None listed

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