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Randomised trial of four to six week follow ups vs no medical follow up after uncomplicated cataract extraction

Randomised trial of four to six week follow ups vs no medical follow up after uncomplicated cataract extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13156311
Enrollment
400
Registered
2014-04-24
Start date
2014-02-03
Completion date
Unknown
Last updated
2019-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eyes ? Cataract extraction Eye Diseases

Interventions

Pathway 1 (standard clinical intervention): Patients reviewed at 6 weeks (+/- 1 week) as is our normal practice and recalled for a further evaluation if deemed appropriate. Patients will be instructed

Sponsors

South Devon Healthcare NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults aged >= 40 years 2. Scheduled for day-case cataract surgery 3. Able to give informed consent

Exclusion criteria

Exclusion criteria: 1. Unable to provide written informed consent 2. Unable to visit their optometrist post-operatively 3. Patients with ocular comorbidity that may be affected by cataract surgery or who require monitoring within 3 months of their operation (including significant diabetic retinopathy, wet age-related macular degeneration (AMD) on treatment, severe/end stage glaucoma, previous retinal detachment or vitrectomy) 4. Patients undergoing another simultaneous ophthalmic procedure 5. Patients who suffer from an intra-operative complication requiring early post-operative evaluation (identified at surgery)

Design outcomes

Primary

MeasureTime frame
1. The primary outcome is corrected distance visual acuity (VA). The primary end point will be VA after 3 months of follow up 2. The primary outcome vision-related quality of life impairment measures are the VCM1 and catquest questionnaires after 3 months of follow up

Secondary

MeasureTime frame
1. Post-operative complication rate difference between the two groups 2. Post-operative patient satisfaction between the two groups at 3 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026