Aqueous Mushroom Extract and Intraocular Pressure (AME)

November 23, 2009 updated by: University of Benin

Aqueous Mushroom Extract as a Glaucoma Agent

The purpose of this study is to determine the effect of Aqueous mushroom extract (AME) on intra ocular pressure (IOP) in humans or as a potential anti glaucoma drug.

Study Overview

Status

Unknown

Conditions

Detailed Description

The Prophet of Islam (Peace Be On Him) was reported to have said that 'mushroom are like manna and their water heals eye diseases'(Sahih Bukhari 1985). This statement is being investigated in view of the link between blood pressure and intra ocular pressure.

Glaucoma which is a sight threatening disease and is associated with raised intraocular pressure has been treated for a long time with beta blockers. Nowadays the drugs of choice are prostaglandin analogs. This study seeks to discover the effect of pleurotus tuberregium on raised intraocular pressure and to compare its effect on I.O.P with that of known glaucoma drugs. This study also seeks to find out at what concentration pleurotus is effective significantly on raised intraocular pressure

Clinical Investigation will be conducted in the Ophthalmological unit of UBTH in two phases. In the first phase 21 relatively young healthy subjects aged less than 50 yrs will be recruited for this study after their informed consent. They will have no previous systemic or ocular diseases and have an intraocular pressure of 19mmHg or less and a visual acuity of 6/6. Base line investigations will include the systolic and diastolic blood pressure, horizontal pupillary diameter and applanation tonometry. The subjects will be divided into three groups of seven each (A1, A2 and A3).

The study will at first constitute two weeks mushroom treatment, two weeks no mushroom treatment and then two weeks mushroom treatment. Treatment will be with aqueous extract of Oyster Medicinal mushroom Extract (4g/100ml) dose: п gutt tid x 1/52 for A1, 2g/100ml dose: п gutt tid x 1/52 for A2 and 1g/100ml dose: п gutt tid x 1/52 for A3. Investigations of the baseline parameters will be done at the start and after each seven days. The subjects will be monitored to ensure full compliance with the designed protocol.

The second phase will involve an equal number of age matched ocular hypertensive or glaucoma patient undergoing treatment in UBTH. They will also be divided into three groups of seven each and the treatment regimen above repeated. The IOP in this case will be taken by a masked observer.

Study Type

Interventional

Enrollment (Anticipated)

42

Phase

  • Phase 2
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Edo
      • Benin City, Edo, Nigeria
        • Eye Clinic University of Benin Teaching Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • clinical diagnosis of open angle glaucoma
  • intraocular pressure above 23mmHg

Exclusion Criteria:

  • close angle glaucoma
  • end stage of glaucoma visual field loss
  • ocular disease other than glaucoma that will interfere with result

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: A1 (glaucoma)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52
Experimental: A2 (glaucoma)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52
Experimental: A3 (glaucoma)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52
Experimental: A1 (normals)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52
Experimental: A2 (normals)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52
Experimental: A3 (normals)
4g/100ml) dose: п gutt tid x 1/52
(2g/100ml) dose: п gutt tid x 1/52
(1g/100ml) dose: п gutt tid x 1/52
(4g/100ml) dose: п gutt tid x 1/52

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
DECREASE INTRA OCULAR PRESSURE
Time Frame: 3 months
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: VINCENT I IYAWE, MD, PhD, University of Benin, Benin City Nigeria

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Akinlabi GA, Igbinigie EV, Akpaja EO, Iyawe VI. Preliminary study on the effect of medicinal mushroom extract and timolol maleate on dexamethasone induced ocular hypertension in feline's eye model.Journal of Medicine and Biomedical Research 6(2)63-68. Akinlabi GA, Uzibor HI, Iyawe IO, Iyawe VI. Effect of oyster mushroom exract(pleurotus ostreatus) and latanoprost on intra ocular pressure using cat's eye model. Journal of Medicine and Biomedical Research 8(1)58-64.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2009

Primary Completion (Anticipated)

February 1, 2010

Study Completion (Anticipated)

February 1, 2010

Study Registration Dates

First Submitted

November 19, 2009

First Submitted That Met QC Criteria

November 19, 2009

First Posted (Estimate)

November 20, 2009

Study Record Updates

Last Update Posted (Estimate)

November 25, 2009

Last Update Submitted That Met QC Criteria

November 23, 2009

Last Verified

November 1, 2009

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MRLLSAW

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Glaucoma

Clinical Trials on OME

Subscribe