Skip to content

Pharmacokinetics and Dynamics of Dexmedetomidine as Adjuvant in TAP Block

Pharmacokinetics and Dynamics of Dexmedetomidine as Adjuvant in TAP Block for Patient Undergoing Lower Abdominal Surgery

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03328299
Enrollment
24
Registered
2017-11-01
Start date
2017-11-11
Completion date
2019-09-01
Last updated
2020-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief summary

TAP-block has been shown to be a safe and effective postoperative analgesia method in a variety of general. Dexmedetomidine is a selective α2 agonist with 8 times more affinity for α2 adrenergic receptors compared to clonidine and possesses all the properties of α2 agonist without respiratory depression. Dexmedetomidine has been focus of interest for its broad spectrum (sedative, analgesic and anesthetic sparing) properties, making it a useful and safe adjunct in many clinical applications.

Interventions

DRUGDexmedetomidine

20 ml of 0.5 % bupivacaine plus dexmedetomidine 1 μg•kg-1

DRUGbupivacaine

20 ml of 0.5 % bupivacaine

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* 24 ASA I-II * patients (age 18-60 years * weight 50-89 kg

Exclusion criteria

* a known allergy to the study drugs * significant cardiac * respiratory, renal or hepatic diseases * bleeding diathesis

Design outcomes

Primary

MeasureTime frameDescription
measure dexmedetomidine level into systemic circulation after local administrationup to 6 hoursassessment of systemic dexmedetomidine level after local administration in TAP block after 15 minutes after giving the block, 30 min, 45 min, 1hrs, 2hrs, 4hrs and 6

Secondary

MeasureTime frameDescription
total dose of IV PCA morphine consumption in the first 24 h postoperative24 hourspostoperative morphine consumption

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026