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Not Yet RecruitingNCT06839391

Effect of Hyaluronidase in Different Doses Added to Bupivacaine on TAB Block Quality During CS

Status
Not Yet Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Benha University · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Accepted

Summary

evaluate the efficacy of hyaluronidase in different doses as an adjuvant to bupivacaine in ultrasound-guided TAB block during CS

Detailed description

Hyaluronidase acts by catalyzing the hydrolysis of hyaluronan, decreased its viscosity, and enchasing the tissue permeability. So, this makes it a suitable additive for other drugs to speed up their distribution and delivery especially in ophthalmic surgery. Several studies showed that multiple injection techniques of TAB block were more successful with a faster onset of anesthesia and higher success rates, with a change in the incidence of complications. This double-blinded randomized prospective study was conducted to evaluate the efficacy of hyaluronidase in different doses as an adjuvant to bupivacaine in ultrasound-guided TAB block during CS . The primary outcome of this study was the duration of sensory block, while secondary outcomes included the onset of sensory block, success rate, total doses of intraoperative rescue analgesia, number of patients needed for postoperative rescue analgesia, and complications.

Conditions

Interventions

TypeNameDescription
DRUGHyaluronidaseEffect of hyaluronidases in different doses added to bupivacaine on quality of ultrasound-guided TAB block during CS ,

Timeline

Start date
2025-03-01
Primary completion
2026-03-01
Completion
2026-04-01
First posted
2025-02-21
Last updated
2025-02-21

Source: ClinicalTrials.gov record NCT06839391. Inclusion in this directory is not an endorsement.