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Dexamethasone as an Adjuvant in Supraclavicular Block

A

Assiut University

Status and phase

Unknown
Phase 2

Conditions

Dexamethasone Efficacy as an Adjuvant in Supraclavicular Block

Treatments

Drug: Dexamethasone injection

Study type

Interventional

Funder types

Other

Identifiers

NCT04345588
Dexamethasone as an Adjuvant

Details and patient eligibility

About

The use of dexamethasone perineurally along with local anesthetic has been shown to improve the duration of analgesia .

Full description

Acute postoperative pain can be effectively controlled with the use of peripheral nerve blocks. Use of additives further prolongs the duration of analgesia For upper limb surgeries below shoulder joint, the brachial plexus block using supraclavicular approach introduced by Kulenkampff has gained popularity. Supraclavicular approach to brachial plexus block is useful for procedures done at or below the level of elbow.

This technique involves the deposition of local anesthetic near the brachial plexus approached from immediately above the clavicle. Brachial plexus is formed by ventral rami of C5, C6, C7, C8, and T1 which forms the roots.These then continue distally to form trunks, divisions, cords,and branches Local anesthetics used alone in supraclavicular block provide analgesia for 4-8 h.

The use of dexamethasone perineurally along with local anesthetic has been shown to improve the duration of analgesia. Intravenous dexamethasone is also useful in attenuating the postoperative need for analgesics in different clinical settings even in the absence of any nerve blocks.

Hence, it is logical to compare the duration of analgesia with the use of dexamethasone in the setting of supraclavicular brachial plexus block, dexamethasone given either perineurally or intravenously.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Patients between 18 and 60 years of age 2. Both male and female gender 3. ASA physical status Classes I and II patients 4. Patients posted for upper limb surgery below shoulder.

Exclusion criteria

    1. Patient refusal 2. Patients with bleeding disorders and those on anticoagulant therapy 3. History of allergy to local anesthetics 4. Infection at the site of block 5. Neuro deficit involving brachial plexus 6. Pregnant women 7. Patients with psychiatric behavior 8. ASA physical status Classes III and IV patients

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

group received dexamethasone perineural
Active Comparator group
Description:
injection dexamethasone 0.05 mg/kg perineural.
Treatment:
Drug: Dexamethasone injection
group received dexamethasone intravenous
Active Comparator group
Description:
injection dexamethasone 0.05 mg/kg intravenously.
Treatment:
Drug: Dexamethasone injection

Trial contacts and locations

0

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Central trial contact

Islam Mohamed Abdel Hamid, post graduated; Ahmed Mohamed Abdel Moteleb, lecturer

Data sourced from clinicaltrials.gov

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