Ptosis, Eyelid Clinical Trial
Official title:
Comparison of Different Surgical Treatments for Severe Ptosis Correction RCT Study
Verified date | April 2019 |
Source | Shanghai Jiao Tong University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Main research purposes of this research is to compare the therapeutic effect and safety of
the superior levator muscle shortening combined with the tarsus resection and the traditional
frontal muscle flap in the correction of severe ptosis.
Aside of above we also tend to explore the dose-effect relationship between the amount of
levator muscle shortened/ tarsus resection and postoperative ptosis correction amount.So as
to develop a more critical and specific guidelines for clinical treatment of ptosis.
So during the research we will recruiting patients with severe ptosis and randomly divide
them into levator muscle and tarsus group and frontal muscle flap group, and follow up those
patient 6 months post operation so as to evaluate the amount of correction and the
side-symptoms.
Status | Enrolling by invitation |
Enrollment | 100 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 3 Years to 80 Years |
Eligibility |
Inclusion Criteria: - unilateral ptosis patient - the levator muscle strength less than 4mm - primary surgery - older than 3 years - ocular rectus muscle of good strength; Exclusion Criteria: - patients who had undergone ptosis correction surgery - patients with neurological ptosis, senile ptosis or pseudo ptosis - patients with abnormal ocular function - patients with Marcus-Gunn syndromes - patients with severe systemic disease or intolerant to general anesthesia - patients or their parents cannot finish follow-up due to educational level or various other reasons. |
Country | Name | City | State |
---|---|---|---|
China | Shanghai Ninth People's Hospital, Affliated to Shanghai Jiao Tong University School of Medicine | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai Jiao Tong University School of Medicine |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | levator muscle's strength | Measuring the muscle strength: let the patient look straight ahead, the examiner presses the eyebrow arch horizontally with the thumb, interrupting the connection between the frontal muscle and the upper eyelids, and ask patient to look down. Then ask the patient to look up as much as they can, and the scale of this movement is the levator muscle strength. When a normal person does not use the frontal muscle, the average scale of the upper eye lids movement is 13.37±2.55mm. The muscle strength of the upper eye lids is generally divided into three levels. The good upper eye lids movement scale is 8mm, the medium is 4~7mm, and the weak one is 0~3mm. |
6 months post the treatment | |
Primary | width of eyes | Measure the width of eyes while doctor shall make sure patient avoid looking up or using the frontal muscle to lift eyelids. | 6 months post the treatment | |
Primary | MRD (margin reflex distance) | Measure the distance from the upper temporal margin to the point of reflection at the center of the cornea, while doctor shall make sure patient avoid looking up or using the frontal muscle to lift eyelids. | 6 months post the treatment | |
Secondary | Numbers of patients not completely corrected | Patients who are below: overcorrection(could result in the inability to close the eye completely) inadequate correction; recurrence of ptosis; All above is based on outcome 1,2,3 |
6 months post the treatment | |
Secondary | Numbers of patients having dry eye syndrome | using OSDI test to see if patients have dry eye syndrome | 6 months post the treatment | |
Secondary | Numbers of patients having corneal injury | corneal injury using topography to check | 6 months post the treatment | |
Secondary | Numbers of patients having orbital insufficiency | orbital insufficiency, using new national standard visual acuity chart to test | 6 months post the treatment | |
Secondary | Numbers of patients having conjunctival prolapse; | based on examination result using slit-lamp microscope | 6 months post the treatment | |
Secondary | Numbers of patients having trichiasis; | based on examination result using slit-lamp microscope | 6 months post the treatment | |
Secondary | Numbers of patients having eye infection; | based on examination result using slit-lamp microscope | 6 months post the treatment |
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