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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04475757
Other study ID # DSREC-02/2018_05
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 15, 2018
Est. completion date June 1, 2020

Study information

Verified date August 2020
Source Dubai Health Authority
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

COMBINED ULTRASOUND GUIDED POSTERIOR TRANS VERSUS ABDOMINAL PLANE & LATERAL FEMORAL CUTANEOUS NERVE BLOCKS FOR POSTOPERATIVE ANALGESIA AFTER HIP HEMIARTHROPLASTIC SURGERY


Description:

TO EVALUATE THE EFFECTIVENESS OF POSTOPERATIVE ANALGESIA FOR HIP HEMIARTHROPLASTIC SURGERIES BY USING ULTRASOUND GUIDED POSTERIOR TRANS VERSUS ABDOMINAL PLANE & LATERAL FEMORAL CUTANEOUS NERVE BLOCKS


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Hemiarthroplaty surgery

- ASA 1 - ASA 4

Exclusion Criteria:

- ALLERGIC TO LOCAL ANESTHETICS

- PATIENT REFUSAL

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Arab Emirates Dubai Health Authority Dubai

Sponsors (1)

Lead Sponsor Collaborator
Dubai Health Authority

Country where clinical trial is conducted

United Arab Emirates, 

Outcome

Type Measure Description Time frame Safety issue
Primary PAIN MANAGEMENT POSTOPERATIVE ANALGESIA 2 DAYS
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