CClinicalTrials.gg
Status unknownNCT01297816minocyclin &RDUpdated Feb 17, 2011

Evaluation of Neuroprotective Effect of Minocycline

A Phase 2 interventional study of placebo and Minocycline in Retinal Detachment, sponsored by Shahid Beheshti University of Medical Sciences. Status unknown at 1 site in Iran, Islamic Republic of. Open to participants aged 8 Years and older. Per ClinicalTrials.gov, last updated 2011-02-17.

Sponsored by Shahid Beheshti University of Medical Sciences · Phase 2, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Dec 2010), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Allocation
Randomized
Ages
8 Years and older
Sex
All
01

Study summary

This process appears as a incredible and progressive event that will not stop till reattachment of RPE and neurosensory retina happened .

Process of degeneration begins from first hours of RD (Retinal Detachment) establishment Neuroprotection of photoreceptor following RD is a novel and debatable discussion encountered in recent years .

How to stop this phenomena and neuroprotective agent role in this issue are a new interest of researcher.

In the study the investigators are planning to perform a clinical trial to demonstrate the minocycline neuroprotective effect in a double blind design as this impact has been implicated previously in a animal study

02

Conditions studied

  • Retinal Detachment

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03

In context

Retinal Detachment

207 studies on the registry are indexed under Retinal Detachment; 27 are open to participants now.

Browse Retinal Detachment studies →

Lead sponsor

Shahid Beheshti University of Medical Sciences is the lead sponsor of 221 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • age over 8 years old
  • gender of both sex
  • normal liver and renal function
  • informed consent received from all patients
  • no pregnancy and no lactation
  • minimal sun exposure

Exclusion criteria

Exclusion Criteria:

  • old RD
  • diabetic retina
  • previous retinal surgery CRF\& liver disfunction RD + PVR > B Hyper sensitivity to tetracycline History previous MPC or PRP Patients unsuccessful SB (retina is off )
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Single group
Masking
Double (Participant, Investigator)

Study arms

  • Placebo comparator
    placebo

    100mg-

    Drug: placebo

  • Placebo comparator
    minocyclin

    Drug: Minocycline

Interventions

  • Drugplacebo

    100mg,BD, fo three month

  • DrugMinocycline

    100mg

06

What researchers measure

Primary outcomes

  1. BCVA

    outcome method of measurement: Snellen chart

    Time frame: changes of BCVA in 3 month

Secondary outcomes

  1. finding of ERG changes

    outcome method of measurement: ERG( testes)

    Time frame: 3 months

  2. finding of OCT changes

    outcome method of measurement: OCT

    Time frame: 3 months

  3. finding of FAF changes

    outcome method of measurement: FAF( testes)

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
  • Labbafinejad medical center
    Tehran, Iran, Islamic Republic of
    • Mohsen Azarmina, Associate Professor · Contact · labbafi@hotmail.com · 00982122585952
    • Mohsen Azarmina, Associate Professor · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01297816
Lead sponsor
Shahid Beheshti University of Medical Sciences
First posted
Feb 17, 2011
Start date
Dec 2010
Primary completion
Dec 2010 (estimated)
Completion
Apr 2011 (estimated)
Last update
Feb 17, 2011

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2010. You cannot join it, but the record below documents what was studied.

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