Unknown PHASE4 INTERVENTIONAL 2-arm NCT04346095

Oral Sedation in Vitreoretinal Surgery

Comparative Analysis of Oral Sedation Versus Standard Intravenous Sedation in Vitreoretinal Surgery With Topical Anesthesia and Sub-tenon's Block

Sponsor: Rocky Vista University, LLC

Conditions Epiretinal Membrane Intraocular Lens Dislocation Intraocular Lens Opacification Macular Holes Retinal Detachment Vitrectomy Vitreous Detachment Vitreous Hemorrhage

Interventions Intravenous Sedatives with or Without Analgesia Oral Sedatives with or Without Analgesia

Updated 5 times since 2020 Last updated: Apr 14, 2020 Started: Jun 30, 2020 Primary completion: Oct 31, 2020 Completion: Nov 30, 2020

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE4 clinical study on Epiretinal Membrane and Intraocular Lens Dislocation, this trial is ongoing. The trial is conducted by Rocky Vista University, LLC and has accumulated 5 data snapshots since 2020. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Unknown PHASE4
Jul 2024 — Sep 2024 [monthly]

Unknown PHASE4

Status: Unknown Status → Unknown
May 2022 — Jul 2024 [monthly]

Unknown Status PHASE4

Status: Not Yet Recruiting → Unknown Status
Jan 2021 — May 2022 [monthly]

Not Yet Recruiting PHASE4
May 2020 — Jan 2021 [monthly]

Not Yet Recruiting PHASE4

First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Rocky Vista University, LLC

Data source: Rocky Vista University, LLC

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

No location information available.