Ocular Complications of Mpox in the Democratic Republic Congo
- Conditions
- MonkeypoxMpox (Monkeypox)
- Registration Number
- NCT06579885
- Lead Sponsor
- Institute of Tropical Medicine, Belgium
- Brief Summary
This is an observational study in which patients diagnosed with mpox will be enrolled, will undergo standard ophthalmological examinations of their eyes to see if there are any complications of mpox. The study will primarily assess the presence of ophthalmological signs and symptoms at enrollment.
- Detailed Description
This is an observational study in which patients diagnosed with mpox will be enrolled in two clinics in remote settings in the DR Congo (Tunda and Kole general hospital) where mpox outbreaks are ongoing. After providing informed consent, participants will undergo standard ophthalmological examinations of their eyes to see if there are any complications of mpox. This includes history taking, clinical examination, technical examinations such as a dilated fundoscopic exam, a fluorescein test and a Schirmer test, and a conjunctival swab for tear collection for monkeypox virus (MPXV) detection. Pictures of the anterior and posterior segment will also be taken to aid later verification and interpretation of the study findings. If they are hospitalised for mpox (for clinical reasons or as part of their participation in another ongoing clinical trial at the study sites), they will be followed up for 14 days and examined during an unscheduled visit in the case of new or worsening severe issues. Otherwise, patients are followed up at day 14 (for those hospitalised), day 28 and day 59. Study participants will receive the same supportive eye care as non-study participants. Study participants will be compensated for their time lost and for transportation to the clinic.
The study will primarily assess the presence of ophthalmological signs and symptoms at enrollment, but also aims to describe the complications of mpox that may arise after that point in time.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 62
- Patient of any age or gender with laboratory-confirmed infection with MPXV
- Laboratory confirmation of MPXV infection less than 48 hours before inclusion
- Patient or culturally acceptable representative is willing and able to give informed consent or assent for participation in the study
- Patients for whom, in the judgment of the recruiting physician, participation in the study would interfere with routine optimal clinical care.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Composite presence or absence of eye disease and visual deficiencies at presentation At enrollment Composite presence of
* orbital lesions (exophthalmos, enophthalmos, oculomotor paralysis...)
* affection of the adnexa
* affection of the anterior segment
* affection of the posterior segment
* affection of the optic nerve
- Secondary Outcome Measures
Name Time Method Ocular signs & symptoms at presentation and during follow-up From enrollment until last follow-up Presence or absence of individual symptoms and signs over time
Visual acuity at presentation and during follow-up From enrollment until last follow-up Result of Optotype letters/numbers and/or E test over time
presence of MPXV in tear fluid at presentation and during follow-up From enrollment until last follow-up Result of MPXV-Polymerase Chain Reaction (PCR) on conjunctival swabs over time
Trial Locations
- Locations (1)
Kamituga General Hospital
🇨🇩Kamituga, South-Kivu Province, Congo, The Democratic Republic of the