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Observation of the Efficacy of Different Vitrectomy Systems to Treat Proliferative Diabetic Retinopathy

Primary Purpose

Proliferative Diabetic Retinopathy, Vitrectomy

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
beveled 27G+ vitrectomy system
standard 25G+ vitrectomy system
Sponsored by
Tianjin Medical University Eye Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Proliferative Diabetic Retinopathy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with vitreous hemorrhage and tractional retinal detachment (TRD) confirmed by fundus image and B ultrasound examination, consistent with the diagnosis of severe proliferated diabetic retinopathy (PDR).
  2. Patient that could follow up postoperatively at the clinic for 6 months more.
  3. All the surgeries were performed by one well-experienced retinal surgeon.

Exclusion Criteria:

  1. Corneal lesions affecting operative field, such as corneal opacity or scar; History of vitreoretinal surgery;
  2. External eye infections;
  3. History of systemic thromboembolism;
  4. Uncontrolled hypertension or hyperglycemia;
  5. Coagulation abnormalities or currently using anticoagulant drugs other than aspirin;
  6. Unable to meet postoperative position requirements;
  7. Unable to be followed up regularly.

Sites / Locations

  • Tianjin Medical University Eye Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

beveled 27G+ group

25G+ group

Arm Description

The group of patients underwent vitrectomy with a beveled 27G+ vitrectomy system.

The group of patients underwent vitrectomy with a standard 25G+ vitrectomy system.

Outcomes

Primary Outcome Measures

the convenience in operating
The convenience will be indicated by times of ancillary instrument using, which evaluated based on the recorded surgical video.
the efficiency of stripping membrane
It will be measured by the area of membrane removed per minute by probe.

Secondary Outcome Measures

best corrected visual acuity (BCVA)
BCVA using a logMAR visual acuity chart method

Full Information

First Posted
June 29, 2022
Last Updated
June 2, 2023
Sponsor
Tianjin Medical University Eye Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05446948
Brief Title
Observation of the Efficacy of Different Vitrectomy Systems to Treat Proliferative Diabetic Retinopathy
Official Title
Comparison of the Efficacy of Standard 25 Gauge (25G)+ and Beveled 27 Gauge (27G)+ Vitrectomy Systems in Proliferative Diabetic Retinopathy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
July 11, 2022 (Actual)
Primary Completion Date
June 1, 2023 (Actual)
Study Completion Date
June 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tianjin Medical University Eye Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In recent years, vitrectomy has moved toward a minimally invasive vitrectomy surgery (MIV) system, which could effectively reduce the occurrence of operation complications, while reducing the time of post-operation recovery. With an improved design of bevel tip and a high cutting rate capacity of 10000cpm, Advanced ULTRAVIT® probes potentially provide an strong technical support for the application of MIV. The new probe facilitates great control during delicate surgical maneuvers, such as separating the hyaloid from the retinal surface, dissecting fibrovascular tissue off the surface of retina. However, there was no sufficient clinical evidence to support the benefits of Advanced ULTRAVIT ® probes in the complicated vitreoretinal surgery, such as proliferative diabetic retinopathy. More importantly, there is an urgent need of clinical evidence to support 10000cpm launch and conversion which is major objective of 2021 VR growth strategies.
Detailed Description
This exploratory study, aiming to demonstrate the beneficial of 27 Gauge probe, which can be flexibly applied as a multifunctional tool for membrane removal by reducing frequencies of switching device, reducing the traction to eyeball during device entering and leaving the eye. Moreover, the outcomes from this study would be an strong evidence to support further comparative study to comprehensively demonstrate the superior function compare to current heavily used 5K 25 gauge probe.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Proliferative Diabetic Retinopathy, Vitrectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
beveled 27G+ group
Arm Type
Experimental
Arm Description
The group of patients underwent vitrectomy with a beveled 27G+ vitrectomy system.
Arm Title
25G+ group
Arm Type
Active Comparator
Arm Description
The group of patients underwent vitrectomy with a standard 25G+ vitrectomy system.
Intervention Type
Device
Intervention Name(s)
beveled 27G+ vitrectomy system
Intervention Description
The device is a novel 27G+ vitrectomy system, whose probe tip is beveled.
Intervention Type
Device
Intervention Name(s)
standard 25G+ vitrectomy system
Intervention Description
The device is a traditional instrument, and its probe tip is flat.
Primary Outcome Measure Information:
Title
the convenience in operating
Description
The convenience will be indicated by times of ancillary instrument using, which evaluated based on the recorded surgical video.
Time Frame
during surgery
Title
the efficiency of stripping membrane
Description
It will be measured by the area of membrane removed per minute by probe.
Time Frame
during surgery
Secondary Outcome Measure Information:
Title
best corrected visual acuity (BCVA)
Description
BCVA using a logMAR visual acuity chart method
Time Frame
baseline to 6 months post-surgery
Other Pre-specified Outcome Measures:
Title
intra-surgery complications
Description
The complications include hemorrhage, iatrogenic retinal breaks, iatrogenic cataracts and occurrence of hypotony during the surgery. They can be detected by a microscope during surgery.
Time Frame
during surgery
Title
Post-operative complications
Description
The complications include recurrent vitreous hemorrhage, retinal detachment, re-operation and ocular hypertension. They can be detected through ophthalmoscope, fundus image, B ultrasound, ophthalmotonometer and so on.
Time Frame
within 6 months after surgery

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with vitreous hemorrhage and tractional retinal detachment (TRD) confirmed by fundus image and B ultrasound examination, consistent with the diagnosis of severe proliferated diabetic retinopathy (PDR). Patient that could follow up postoperatively at the clinic for 6 months more. All the surgeries were performed by one well-experienced retinal surgeon. Exclusion Criteria: Corneal lesions affecting operative field, such as corneal opacity or scar; History of vitreoretinal surgery; External eye infections; History of systemic thromboembolism; Uncontrolled hypertension or hyperglycemia; Coagulation abnormalities or currently using anticoagulant drugs other than aspirin; Unable to meet postoperative position requirements; Unable to be followed up regularly.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Li
Organizational Affiliation
Tianjin Medical University Eye Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tianjin Medical University Eye Hospital
City
Tianjin
ZIP/Postal Code
300386
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Observation of the Efficacy of Different Vitrectomy Systems to Treat Proliferative Diabetic Retinopathy

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