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Trial · NCT02717871

Swiss PACK-CXL Multicenter Trial for the Treatment of Infectious Keratitis

NCT02717871, Phase 3, Completed, University Hospital, Geneva

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Swiss PACK-CXL Multicenter Trial for the Treatment of Infectious Keratitis. Trials, record NCT02717871. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02717871

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Swiss PACK-CXL Multicenter Trial for the Treatment of Infectious Keratitis
NCT number
NCT02717871
Status
Completed
Phases
Phase 3
Enrollment
35 participants, actual
Lead sponsor
University Hospital, Geneva
Conditions
Keratitis; Infectious Disease (Manifestation)
Interventions
PACK-CXL, Cefazolin in combination with either tobramycin or gentamicin, Cycloplegic agents (cyclopentolate 1% eye drops), Fluoroquinolones (Besifloxacin ; ciprofloxacin ; gatifloxacin ; levofloxacin ; moxifloxacin ; ofloxacin ), Corticosteroids (prednisolone acetate 0.5% or 1% eye drops)
First posted
2016-03-24
Last updated
2020-10-20

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTime to re-epithelialization of the corneal surface28 days
SecondaryTime from treatment to discharge of the patient28 days

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers12

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
10406613BACKGROUNDPubMed
10938955BACKGROUNDPubMed
11285665BACKGROUNDPubMed
18408193BACKGROUNDPubMed
18520510BACKGROUNDPubMed
19730094BACKGROUNDPubMed
19772254BACKGROUNDPubMed
21102196BACKGROUNDPubMed
21874347BACKGROUNDPubMed
23941330BACKGROUNDPubMed

1 to 10 of 12

See all 12 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02717871

GET https://conductscience.org/api/trials/v1/NCT02717871/registered