---
title: Correlation Between Preoperative Refraction and Anterior Segment Parameters With ICL Vault
nct_id: NCT05670626
overall_status: ENROLLING_BY_INVITATION
phase: NA
sponsor: Kasr El Aini Hospital
study_type: INTERVENTIONAL
primary_condition: Refractive Errors
countries: Egypt
canonical_url: "https://parkinsonspathways.com/agent/trials/NCT05670626.md"
clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT05670626"
ct_last_update_post_date: 2025-03-13
last_seen_at: "2026-05-12T07:33:08.013Z"
source: ClinicalTrials.gov (mirrored, no enrichment)
---
# Correlation Between Preoperative Refraction and Anterior Segment Parameters With ICL Vault

**Official Title:** Correlation Between ICL Vault and Preoperative Refraction ( Spherical Equivalent) and Anterior Segment Parameters Measured by Optical Biometry and Scheimpflug Imaging

**NCT ID:** [NCT05670626](https://clinicaltrials.gov/study/NCT05670626)

## Key Facts

- **Status:** ENROLLING_BY_INVITATION
- **Phase:** NA
- **Study Type:** INTERVENTIONAL
- **Target Enrollment:** 40
- **Lead Sponsor:** Kasr El Aini Hospital
- **Conditions:** Refractive Errors, Myopia, Myopic Astigmatism
- **Start Date:** 2022-12-14
- **Completion Date:** 2025-12
- **CT.gov Last Update:** 2025-03-13

## Brief Summary

This prospective non-comparative interventional study aims to analyse the pre-operative factors affecting the range of optimal ICL vaulting. the main question is what is the correlation between age, gender, spherical equivalent, white to white, anterior chamber volume and depth and postoperative vault? participants will do preoperative investigations ( specular microscopy, pentacam and biometry ) then refractive surgery (ICL implantation) followed by follow-up visits to assess the post-operative ICL vault and visual outcome.

## Detailed Description

Procedure: Refractive error correction by implantable contact lens ( ICL) will be preceded by a Preoperative assessment of the patient's anterior segment using specular Microscopy, pentacam and biometry and full ophthalmic examination.

Post-operatively, visual acuity evaluation, intraocular pressure, and anterior and posterior segments examination using a slit lamp will be done on days 1 and 3 and then repeated after 1 month and 6 months Assessment of ICL vault measurement using pentacam scheimpflug imaging after 1 and 6 months will be done then a correlation between the ICL vault and the patient's refractive error and preoperative anterior segments parameters will be evaluated

## Eligibility

- **Minimum age:** 21 Years
- **Maximum age:** 45 Years
- **Sex:** ALL
- **Healthy Volunteers:** Yes

```
Inclusion Criteria:

* Age:21 - 45 years old.
* High Myopia or Myopic astigmatism.
* Patients with stable preoperative refraction for the previous 12 months.
* Aqueous depth (ACD internal) = 2.8 mm or greater from the endothelial side using pentacam.
* Patients who are not fit for LASIK.
* No previous intraocular surgeries.

Exclusion Criteria:

* Patients with endothelial cell count \< 2800 cells /mm2
* Patients with corneal opacities
* Patients with preoperative glaucoma, cataract, and retinal disease.
* Patients with any systemic diseases especially collagen diseases.
```

## Arms

- **non comparative interventional study** (OTHER) — patients with high refractive error will do phakic ICL after preoperative assessment of anterior segments parameters and post-operative ICL vault will be measured using pentacam

## Interventions

- **Refractive Surgery** (PROCEDURE) — Phakic implantable contact lens ( ICL)

## Primary Outcomes

- **ICL vault size** _(time frame: 1 month)_ — assessment of ICL vault by scheimpflug image
- **ICL Vault size** _(time frame: 6 months)_ — assessment of ICL vault by scheimpflug image
- **Post Operative UCVA and BCVA** _(time frame: 1-3 days)_ — assessment of Post Operative visual acuity
- **Post Operative UCVA and BCVA** _(time frame: 1 month)_ — assessment of Post Operative visual acuity
- **Post Operative UCVA and BCVA** _(time frame: 6 months)_ — assessment of Post Operative visual acuity
- **Post Operative IOP** _(time frame: 1 - 3 days)_ — assessment of post operative intraocular pressure
- **Post Operative IOP** _(time frame: 1 month)_ — assessment of post operative intraocular pressure
- **Post Operative IOP** _(time frame: 6 month)_ — assessment of post operative intraocular pressure

## Locations (1)

- Alwatany Eye Hospital, Cairo, Cairo Governorate, Egypt

## Recent Field Changes (last 30 days)

- `sponsor.lead` — added _(2026-05-12)_
- `results.hasResults` — added _(2026-05-12)_
- `locations.alwatany eye hospital|cairo|cairo governorate|egypt` — added _(2026-05-12)_
- `status.overallStatus` — added _(2026-05-12)_
- `status.primaryCompletionDate` — added _(2026-05-12)_
- `status.completionDate` — added _(2026-05-12)_
- `status.lastUpdatePostDate` — added _(2026-05-12)_
- `design.phases` — added _(2026-05-12)_
- `design.enrollmentCount` — added _(2026-05-12)_
- `eligibility.criteria` — added _(2026-05-12)_
- `eligibility.minAge` — added _(2026-05-12)_
- `eligibility.maxAge` — added _(2026-05-12)_
- `eligibility.sex` — added _(2026-05-12)_
- `outcomes.primary` — added _(2026-05-12)_
- `armsInterventions.arms` — added _(2026-05-12)_
- `armsInterventions.interventions` — added _(2026-05-12)_

---

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*Source data (authoritative): https://clinicaltrials.gov/study/NCT05670626*  
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