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Post-operative Satisfaction With Glaucoma Surgery Trial

Sun Yat-sen University logo

Sun Yat-sen University

Status

Withdrawn

Conditions

Glaucoma

Treatments

Behavioral: film and trained counseling
Other: traditional counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT01726569
ZOC-CREST1

Details and patient eligibility

About

  1. Investigate degree of postoperative satisfaction in county level hospital glaucoma patients.
  2. Investigate the effect of educational intervention affect the degree of satisfaction in glaucoma patients.
  3. Investigate the effect factors of postoperative satisfaction.

Full description

Glaucoma is the leading cause irreversible blindness worldwide, but only less than 10% glaucoma patients were diagnosed in the country of Asia areas. In the country of China, patients who are low educational level and less known acknowledgement and information have less known glaucoma. In the help of the government and some international non-governmental organizations(NGOs), a lot of people in the country know the cataract, and the operability of cataract is increase. Because vision loss usually development after operation for glaucoma. If patients did not understand this, they may be not only do not accept operation, but also affect operability of cataract. We hope the educational intervention for glaucoma can increase the degree of satisfaction in glaucoma patients.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age≥18 years, glaucoma patients who do the peripheral iridectomy or trabeculotomy

Exclusion criteria

  • patients who had been the trabeculotomy, vision≤0.05, severe psychotic disorders and dysgnosia

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

film and trained counseling
Experimental group
Description:
Subjects will be asked to watch a 5-10 min film and participate in a 10-15 min pre-operative counseling session with a trained doctor/nurse. Subjects will also participate in a 5 min post-operative counseling session and follow up counseling after operation 1 week and 6 weeks
Treatment:
Behavioral: film and trained counseling
Other: traditional counseling
traditional counseling
Other group
Description:
Subjects will be participate or not participate in pre-operative counseling and/or post-operative counseling with a rural hospital's doctor/nurse.
Treatment:
Other: traditional counseling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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