Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06638827
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-06
Brief Title:
Outcome of Bilateral Thoracoscopic Sympathectomy for Patients with Primary Focal Hyperhidrosis
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Outcome of Bilateral Thoracoscopic Sympathectomy for Patients with Primary Focal Hyperhidrosis Sohag University Hospital Experience
Status:
RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to examine the overall efficiency of Bilateral Thoracoscopic Sympathectomy on the permanent reduction of Primary focal hyperhidrosis of predilective parts of the body palms armpits face and soles
Detailed Description:
The aims of this study are
1 examine the efficiency of Bilateral Thoracoscopic Sympathectomy BTS with different levels of transection among the persons with the Primary focal Hyperhidrosis PFH
2 examine the influence of BTS on cardio-pulmonary function tests in persons with PFH after the operation
3 examine the incidence duration and intensity of compensatory sweating after BTS among persons with PFH
4 examine the incidence duration localization and treatment of postoperative pain after BTS among persons with PFH
5 determine postoperative complications of BTS among persons with PFH
6 examine the influence of BTS on quality of life among persons with PFH
1 examine the efficiency of Bilateral Thoracoscopic Sympathectomy BTS with different levels of transection among the persons with the Primary focal Hyperhidrosis PFH
2 examine the influence of BTS on cardio-pulmonary function tests in persons with PFH after the operation
3 examine the incidence duration and intensity of compensatory sweating after BTS among persons with PFH
4 examine the incidence duration localization and treatment of postoperative pain after BTS among persons with PFH
5 determine postoperative complications of BTS among persons with PFH
6 examine the influence of BTS on quality of life among persons with PFH
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None