Comparison of Different Doses of Verteporfin Photodynamic Therapy in the Treatment of Chronic Central Serous Chorioretinopathy

Status: Unknown
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a prospective, randomized and controlled clinical trial of photodynamic therapy (PDT) for chronic central serous chorioretinopathy (CSC). The patients who met the inclusion criteria were randomly divided into 50% dose PDT treatment group and 70% dose PDT treatment group. The primary treatment success rate and adverse event rate of the two groups were compared by optical coherence tomography (OCT), and then the best PDT treatment scheme for chronic CSC was summarized.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• 18-75 years old, regardless of gender;

• Meet the diagnostic criteria of central serous chorioretinopathy;

• The course of CSC (subject to the symptoms of this disease) is more than 3 months;

• Patients with simultaneous diseases of both eyes were included in those with more subretinal fluid.

Locations
Other Locations
China
Peking University People's Hospital
RECRUITING
Beijing
Contact Information
Primary
Yuou Yao, Dr
yaoyoyo19@139.com
13651177854
Backup
Mingwei Zhao, Dr
dr_mingweizhao@163.com
13801057408
Time Frame
Start Date: 2020-01-01
Completion Date: 2023-12-31
Participants
Target number of participants: 100
Treatments
Experimental: 50% dose of PDT
Patients received 50% dose of verteporfin PDT therapy.
Experimental: 70% dose of PDT
Patients received 70% dose of verteporfin PDT therapy.
Related Therapeutic Areas
Sponsors
Leads: Peking University People's Hospital

This content was sourced from clinicaltrials.gov