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NCT05841251

Phenylephrine Versus Tranexamic Acid to Control Bleeding in Patients Undergoing Inferior Turbinoplasty by Coblation

Status unknown NA Last updated 3 May 2023
What this trial tests

NA trial testing Topical Phenylephrine Solution in Intraoperative Bleeding in 80 participants. Status unknown.

Timeline
1 May 2023
Primary endpoint
1 September 2023
1 December 2023

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment80
Start date1 May 2023
Primary completion1 September 2023
Estimated completion1 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 60, any sex, with Intraoperative Bleeding or Coblation Turbinoplasty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Coblation is a unique method of delivering radio frequency energy to the soft tissue for applications in otolaryngology. It induces reduction of the inferior turbinate by vaporizing and destroying the soft erectile tissue. The volume reduction and tissue fibrosis are immediate and sustainable. Bleeding from the vascular capillary beds of the sinonasal mucosa compromises the surgical field and increases operative time and risk of complications. In this study we try to assist hemostasis with a multifaceted approach, including use of topical vasoconstrictors "phenylephrine" and systemic antifibrinolytic agent "tranexamic acid".

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Topical Phenylephrine Solution

Trials testing the same drug.

Other recruiting trials for Intraoperative Bleeding

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing