- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01295853
T3 Versus T4 Sympathicotomy for Treatment of Primary Palmar Hyperhidrosis
T3 Versus T4 Sympathicotomy for Treatment of Primary Palmar Hyperhidrosis: a Prospective Randomized Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Palmar hyperhidrosis (PH) is a benign sympathetic disorder that does not threaten health but affects daily activities, and may causes social withdrawal and even depression.1 An incidence of up to 1% has been reported by various series in the literature. The incidence in men and women is the same; however women are more likely to seek medical attention, which may explain the higher incidence of female patients in most surgical series [2,3]. Although various treatment options are available, including topical and systemic therapies, iontophoresis, regional nerve block, and botulinum toxin injection, each has its limitations 4. Video-assisted thoracoscopic sympathetic surgery is currently a worldwide accepted treatment of primary palmar hyperhidrosis (PH) 5. However, compensatory hyperhidrosis (CH) is the most common and serious side effect that occurs in 30-70% of patients after T2 or T2-3 sympathectomy 6. For that now T2 sympathetic surgeries are seldom used in PH. Procedures that involve T3 or/and T4 sympathetic ganglions are widely accepted in many centers with favourable results.5 But some patients still present with certain degrees of CH or over dry hands after operation 7, 8.
The aim of this study is to compare the two methods for the treatment of PH, in which the sympathetic chain was transected in merely one segment, on the level of either the third or the fourth ribbed, defined as T3 sympathicotomy or T4 sympathicotomy, respectively. Emphasis was placed on the evaluation of the efficacy, side effects, and patients' satisfaction rate to these two types of surgical therapy.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Mansoura, Egypt, 35111
- Mansoura University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with primary palmar hyperhidrosis
Exclusion Criteria:
- Patients with pleural adhesion
- Bleeding diathesis
- Local infection
- Patients with certain anatomic anomalies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: t3 sympathicotomy
The sympathetic chain was identified at the level of the crossing of the third or fourth costal heads after dissection of the parietal pleura and completely divided about 1 cm wide at the upper margin of the rib.
With assistance of anaesthesia team we reinflate the lung totally in sequence with removal of the trocars.
The same procedure was performed on the opposite side and ablation of the sympathetic chain overlying the rib was performed bilaterally.
At the end of surgery, a postoperative chest x-ray was routinely taken to rule out pneumothorax or hemothorax.
|
The sympathetic chain was identified at the level of the crossing of the third or fourth costal heads after dissection of the parietal pleura and completely divided about 1 cm wide at the upper margin of the rib.
With assistance of anaesthesia team we reinflate the lung totally in sequence with removal of the trocars.
The same procedure was performed on the opposite side and ablation of the sympathetic chain overlying the rib was performed bilaterally.
At the end of surgery, a postoperative chest x-ray was routinely taken to rule out pneumothorax or hemothorax.
Other Names:
The sympathetic chain was identified at the level of the crossing of the third or fourth costal heads after dissection of the parietal pleura and completely divided about 1 cm wide at the upper margin of the rib.
With assistance of anaesthesia team we reinflate the lung totally in sequence with removal of the trocars.
The same procedure was performed on the opposite side and ablation of the sympathetic chain overlying the rib was performed bilaterally.
At the end of surgery, a postoperative chest x-ray was routinely taken to rule out pneumothorax or hemothorax.
Other Names:
|
|
Active Comparator: t4 sypathicotomy
The sympathetic chain was identified at the level of the crossing of the third or fourth costal heads after dissection of the parietal pleura and completely divided about 1 cm wide at the upper margin of the rib.
With assistance of anaesthesia team we reinflate the lung totally in sequence with removal of the trocars.
The same procedure was performed on the opposite side and ablation of the sympathetic chain overlying the rib was performed bilaterally.
At the end of surgery, a postoperative chest x-ray was routinely taken to rule out pneumothorax or hemothorax.
|
The sympathetic chain was identified at the level of the crossing of the third or fourth costal heads after dissection of the parietal pleura and completely divided about 1 cm wide at the upper margin of the rib.
With assistance of anaesthesia team we reinflate the lung totally in sequence with removal of the trocars.
The same procedure was performed on the opposite side and ablation of the sympathetic chain overlying the rib was performed bilaterally.
At the end of surgery, a postoperative chest x-ray was routinely taken to rule out pneumothorax or hemothorax.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
postoperative compensatory hyperhidrosis
Time Frame: 2008-2010
|
CH remains the most common and distressing complication postsympathicotomy and many efforts have been made to ovoid its happening .Chou et al, 2 suggested that the underlying mechanism of CH may be due to a reflex response in sweating centre in hypothalamus but the exact mechanism beyond this phenomenon remain unclear.
|
2008-2010
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
improvement of planter sweating assessment of overdry hands early postoperative complication ( pneumothorax,,,,,) recurrance
Time Frame: 2008-2010
|
The recurrence rate in T4 group was occurring in 2 patients (2.8%), whereas one recurrence found in T3 group (1.5%). Kim et al 4, reported a 4.2 % of patients undergo T3 sympathicotomy complaining of gustatory sweating in a study carried out on 56 patients. However In our study there was no occurrence of postsympathicotomy gustatory hyperhidrosis and this may be due to the small numbers in our series. |
2008-2010
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: ahmed negm, md, Mansoura University Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AMRO2345
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Recurrence
-
Portuguese Oncology Institute, CoimbraCompletedColorectal Cancer | Recurrence, Local NeoplasmPortugal
-
Chinese PLA General HospitalRecruitingHCC | Recurrence TumorChina
-
Paracelsus Medical UniversityHeinrich-Heine University, Duesseldorf; Poznan University of Medical Sciences; University Hospital of Ferrara and other collaboratorsCompletedToxicity | Local Neoplasm RecurrenceAustria
-
Aarhus University HospitalRecruitingFear of Cancer RecurrenceDenmark
-
Sixth Affiliated Hospital, Sun Yat-sen UniversityCompletedLocal Recurrence of Malignant Tumor of Rectum | Local Re-Recurrence of Malignant Tumor of Rectum
-
General Hospital GroeningeUniversitaire Ziekenhuizen KU Leuven; Jessa Hospital; University Hospital, Ghent and other collaboratorsEnrolling by invitation
-
Saint Petersburg State University, RussiaInstitute of Cytology of the Russian Academy of Sciences; The Russian Science...Active, not recruitingCancer | Anesthesia | Cancer RecurrenceRussian Federation
-
Dallas VA Medical CenterTerminatedSolid Tumors | Cancer RecurrenceUnited States
-
The University of Hong KongHealth and Medical Research FundRecruitingCancer | Fear of Cancer RecurrenceHong Kong
-
German Centre for Assessment and Evaluation of...Not yet recruitingComplication | Continence | Potency | Biochemical RecurrenceGermany
Clinical Trials on t3 sympathicotomy
-
Michiel KuijpersCompleted
-
University of Campania "Luigi Vanvitelli"Completed
-
University of GroningenWithdrawnComplex Regional Pain Syndrome Type I of the Upper LimbNetherlands
-
University Medical Center GroningenRecruiting
-
ZimVieCompletedEdentulous JawUnited States, Italy, Spain
-
Stanford UniversityCompleted
-
Chinese University of Hong KongCompleted
-
Mayo ClinicCompleted
-
ZimVieCompletedEdentulous JawUnited States, Germany