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NCT06400355

Effect of Mannitol on Recovery Pattern After Orthognathic Surgery

Active, enrolled NA Last updated 23 July 2024
What this trial tests

NA trial testing Mannitol in Orthognathic Surgery in 60 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 March 2024
Primary endpoint
1 June 2024
1 August 2024

Quick facts

Lead sponsorNational Cancer Institute, Egypt
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment60
Start date1 March 2024
Primary completion1 June 2024
Estimated completion1 August 2024
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

National Cancer Institute, Egypt

Who can join

Adults 18 to 65, any sex, with Orthognathic Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to test, whether mannitol infusion in different doses will affect recovery pattern? the investigators hypothesized that infusion of mannitol in doses of 0.5 gm/kg before recovery from anesthesia after orthognathic surgery shortens patients' recovery time, and improves recovery quality, as well as postoperative cognitive function better.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Mannitol

Trials testing the same drug.

Other recruiting trials for Orthognathic Surgery

Currently open trials in the same condition.

Other National Cancer Institute, Egypt trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06400355.

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