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Minimally Invasive Surgical Epilepsy Trial for Temporal Lobe Epilepsy (MISET-TLE)

Primary Purpose

Temporal Lobe Epilepsy, Open Surgery, Minimally Invasive Surgery

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Functional anterior temporal lobectomy (FATL)
Anterior temporal lobectomy (ATL)
Sponsored by
First Affiliated Hospital Xi'an Jiaotong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Temporal Lobe Epilepsy focused on measuring Temporal lobe epilepsy, Anterior temporal lobectomy, Functional anterior temporal lobectomy, Randomized controlled trial, Minicraniotomy

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. male or female aged between 18 and 60 years;
  2. drug- resistant temporal lobe epilepsy, remaining seizures after two or more tolerated and appropriately chosen antiepileptic drugs;
  3. monthly or more seizures during the preceding year prior to trial;
  4. the full- scale intelligence quotient (IQ) more than 70, understanding and completing the trial;
  5. signing the informed consent;
  6. good compliance, at least 12- month follow- up after surgery.

Exclusion Criteria:

  1. tumor in temporal lobe;
  2. extratemporal epilepsy and temporal plus epilepsy;
  3. drug- responsive epilepsy, seizure freedom with current drugs in recent one year;
  4. pseudoseizures;
  5. seizures arising from bilateral temporal lobes;
  6. significant comorbidities including progressive neurological disorders, active psychosis, and drug abuse;
  7. a full- scale IQ lower than 70, unable to complete tests;
  8. previous epilepsy surgery;
  9. poor compliance and inadequate follow- up.

Sites / Locations

  • First Affiliated Hospital of Xi'an Jiaotong UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Functional anterior temporal lobectomy (FATL)

Anterior temporal lobectomy (ATL)

Arm Description

FATL via minicraniotomy is a new surgical approach, consisting of amygdalohippocampectomy and the lateral temporal lobotomy.

ATL via large frontotemporal craniotomy is a conventional surgical approach, consisting of amygdalohippocampectomy and en bloc resection of the lateral temporal lobe.

Outcomes

Primary Outcome Measures

Surgery duration
Surgery duration in hours, the time from the beginning of incising the skin to the finish of suturing the skin.
Blood loss
Blood loss in millilitres during the operation.
Skin incision
Length of skin incision in centimetres
Bone flap
Size of bone flap in square centimeter
Postoperative hospital stay
Postoperative hospital stay in days, the time from the first postoperative day to discharge date.
Complications
The incidence of postoperative complications

Secondary Outcome Measures

Seizure outcomes classified by the International League Against Epilepsy (ILAE)
Seizure outcomes are classified by the International League Against Epilepsy (ILAE). Specific seizure classifications: class 1, seizure-free; class 2, only auras, no other seizures; class 3, 1-3 seizure days per year with or without auras; class 4, ≥4 seizure days per year and ≥50% reduction in baseline numbers of seizure days, with or without auras; class 5, <50% reduction and ≤100% increase in baseline numbers of seizure days, with or without auras; class 6, >100% increase in baseline numbers of seizure days, with or without auras. Proportion of each class is calculated.
Seizure outcomes classified by the Engel
Seizure outcomes are also classified by the Engel classification: class 1, free from disabling seizures; class 2, rare disabling seizures (almost seizure free); class 3, worthwhile improvement; class 4, no worthwhile improvement. Proportion of each class is calculated.
Quality of life assessed by the Quality of Life in Epilepsy Inventory- 89
Quality of life is evaluated by the epilepsy- specific Quality of Life in Epilepsy Inventory- 89 (QOLIE- 89). QOLIE-89 is one of the special inventories applied mostly to assess QOL in research protocols, especially in long-term prospective clinical investigations. QOLIE- 89 has 89 items, range of scores, 0 to 100, with higher scores indicating better QOL.

Full Information

First Posted
July 9, 2021
Last Updated
December 28, 2022
Sponsor
First Affiliated Hospital Xi'an Jiaotong University
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1. Study Identification

Unique Protocol Identification Number
NCT05019404
Brief Title
Minimally Invasive Surgical Epilepsy Trial for Temporal Lobe Epilepsy
Acronym
MISET-TLE
Official Title
Functional Anterior Temporal Lobectomy Via Minicraniotomy as a Novel Surgical Therapy for Temporal Lobe Epilepsy: a Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 25, 2023 (Anticipated)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
First Affiliated Hospital Xi'an Jiaotong University

4. Oversight

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

5. Study Description

Brief Summary
Temporal lobe epilepsy (TLE) is a chronically neurological disease characterized by progressive seizures. TLE is the most frequent subtype of refractory focal epilepsy in adults. Epilepsy surgery has proven to be very efficient in TLE and superior to medical therapy in two randomized controlled trials. According to the previous experience, the investigators use functional anterior temporal lobectomy (FATL) via minicraniotomy for TLE. To date, this minimally invasive open surgery has been not reported. The investigators here present a protocol of a prospective trail which for the first time evaluates the outcomes of this new surgical therapy for TLE.
Detailed Description
Temporal lobe epilepsy (TLE) is a chronically neurological disease characterized by progressive seizures, followed by a latency period of several years after various injuries including febrile seizures, infection, trauma, tumors, and vascular malformation. Hippocampal sclerosis is the most common histopathological finding. The macroscopic changes of TLE with hippocampal sclerosis include the diminished size, sclerosis, and reduced metabolism in mesial temporal structures (amygdala, hippocampus, and parahippocampal gyrus). The microscopic changes include neuronal loss, gliosis, and axonal reorganization. As TLE progresses, most of patients become resistant to current antiepileptic drugs. Therefore, TLE is the most frequent subtype of refractory focal epilepsy in adults. Epilepsy surgery has proven to be very efficient for TLE and superior to medical therapy in two randomized controlled trials. Patients with surgical therapy have high seizure-free rate with the range of 60% to 80 % while less than 5% with medical treatment. Anterior temporal lobectomy (ATL) is the most frequently used approach for TLE. For patients with TLE, Engel suggested referral to ATL should be strongly considered. The decision analysis showed that ATL increased life expectancy and quality- adjusted life expectancy in patients with TLE compared with medical management. Nevertheless, ATL is performed by large frontotemporal craniotomy. Although complication rates after temporal lobectomy have decreased dramatically over time, ATL creates a large cavity with temporal lobe resected, causing potential complications such as bleeding, brain shifts and subdural collections. With the advances in minimally invasive surgery, surgical techniques of ATL for TLE need to be continuously improved. For this reason, the investigators modify the surgical approach. Functional anterior temporal lobectomy (FATL) via minicraniotomy is established. Recently, 25 patients with TLE undergoing FATL obtained satisfactory outcomes in our center (unpublished data). To date, this new open surgery for TLE has been not reported. The safety and efficacy of FATL need to be verified. Therefore, the investigators here present a protocol of the minimally invasive surgical epilepsy trial for TLE (MISET-TLE) which for the first time evaluates the outcomes of FATL as a new surgical approach for TLE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Temporal Lobe Epilepsy, Open Surgery, Minimally Invasive Surgery
Keywords
Temporal lobe epilepsy, Anterior temporal lobectomy, Functional anterior temporal lobectomy, Randomized controlled trial, Minicraniotomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
a single-center, prospective, single-blinded, double-arm, randomized, controlled trial
Masking
Outcomes Assessor
Masking Description
Outcomes assessors are blinded to the treatment throughout the entire study. Blinding is maintained by having patients wear large hats during the interview to obscure skin incision and providing patients strict instruction not to reveal treatment arm.
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Functional anterior temporal lobectomy (FATL)
Arm Type
Experimental
Arm Description
FATL via minicraniotomy is a new surgical approach, consisting of amygdalohippocampectomy and the lateral temporal lobotomy.
Arm Title
Anterior temporal lobectomy (ATL)
Arm Type
Active Comparator
Arm Description
ATL via large frontotemporal craniotomy is a conventional surgical approach, consisting of amygdalohippocampectomy and en bloc resection of the lateral temporal lobe.
Intervention Type
Procedure
Intervention Name(s)
Functional anterior temporal lobectomy (FATL)
Intervention Description
Patients are placed in the supine position with the head contralaterally rotated 30°. The 3D model of incision and bone flap is printed prior to surgery by the slicer software based on the MRI data. Slightly curve incision with the length of about 6 cm in the temporal region is marked according to the 3D model. Temporal craniotomy via small bone window with the diameter of about 3 cm is performed. From the temporal pole along T1 about 5 cm posteriorly, temporal horn is opened by dissecting the middle temporal gyrus. The head of temporal horn is exposed. The amygdala is resected. Then, the parahippocampal gyrus and hippocampus are en bloc resected. The lateral temporal lobotomy is easy due to large view following the removal of mesial structures. The lateral posterior temporal lobotomy is no more than 5 cm from the temporal pole.
Intervention Type
Procedure
Intervention Name(s)
Anterior temporal lobectomy (ATL)
Intervention Description
Patients are placed in the supine position with the head contralaterally rotated 30°. Large frontotemporal craniotomy is performed. Question mark-shaped incision with the length of 20- 25 cm in the frontotemporal region is marked. The size of the bone flap is approximately 5×7 cm for the exposure of lateral temporal lobe. ATL consists of en bloc resection of the anterior 5 cm of lateral temporal lobe, followed by the removal of mesial structures including the amygdala, parahippocampal gyrus, and hippocampus.
Primary Outcome Measure Information:
Title
Surgery duration
Description
Surgery duration in hours, the time from the beginning of incising the skin to the finish of suturing the skin.
Time Frame
At the end of the surgery.
Title
Blood loss
Description
Blood loss in millilitres during the operation.
Time Frame
At the end of the surgery.
Title
Skin incision
Description
Length of skin incision in centimetres
Time Frame
At the end of the surgery.
Title
Bone flap
Description
Size of bone flap in square centimeter
Time Frame
At the end of the surgery.
Title
Postoperative hospital stay
Description
Postoperative hospital stay in days, the time from the first postoperative day to discharge date.
Time Frame
Up to 1 month after surgery.
Title
Complications
Description
The incidence of postoperative complications
Time Frame
Up to 1 year after epilepsy surgery
Secondary Outcome Measure Information:
Title
Seizure outcomes classified by the International League Against Epilepsy (ILAE)
Description
Seizure outcomes are classified by the International League Against Epilepsy (ILAE). Specific seizure classifications: class 1, seizure-free; class 2, only auras, no other seizures; class 3, 1-3 seizure days per year with or without auras; class 4, ≥4 seizure days per year and ≥50% reduction in baseline numbers of seizure days, with or without auras; class 5, <50% reduction and ≤100% increase in baseline numbers of seizure days, with or without auras; class 6, >100% increase in baseline numbers of seizure days, with or without auras. Proportion of each class is calculated.
Time Frame
Up to 1 year after epilepsy surgery
Title
Seizure outcomes classified by the Engel
Description
Seizure outcomes are also classified by the Engel classification: class 1, free from disabling seizures; class 2, rare disabling seizures (almost seizure free); class 3, worthwhile improvement; class 4, no worthwhile improvement. Proportion of each class is calculated.
Time Frame
Up to 1 year after epilepsy surgery
Title
Quality of life assessed by the Quality of Life in Epilepsy Inventory- 89
Description
Quality of life is evaluated by the epilepsy- specific Quality of Life in Epilepsy Inventory- 89 (QOLIE- 89). QOLIE-89 is one of the special inventories applied mostly to assess QOL in research protocols, especially in long-term prospective clinical investigations. QOLIE- 89 has 89 items, range of scores, 0 to 100, with higher scores indicating better QOL.
Time Frame
Up to 1 year after epilepsy surgery
Other Pre-specified Outcome Measures:
Title
Intelligence assessed by the Wechsler Adult Intelligence Scale
Description
Intelligence is assessed by the Wechsler Adult Intelligence Scale IV (WAIS-IV). WAIS-IV provides four major domains: perceptual reasoning, processing speed, verbal comprehension, working memory. The WAIS-IV also provides two overall summary scores including a Full-Scale IQ and a General Ability Index (GAI), where FSIQ is a measurement of performance across all subcategories, but the GAI is more resistant to issues that might arise from cognitive impairment, allowing for a more precise and truthful analysis. Higher score means better outcome. Intelligence is classified according to the total score : 1) extremely abnormal with more than 130 points; 2) Exceptional: 120-129 points; 3) Higher than usual: 110-119 points; 4) Normal: 90-109 points; 5) Lower than usual: 80-89 points; 6) Boundary: 70-79 points; 7) Mental Retardation: lower than 69 points.
Time Frame
Up to 1 year after epilepsy surgery
Title
Depression assessed by Beck's Depression Inventory
Description
Beck's Depression Inventory (BDI) with 21 items, range of scores, 0 to 63. Higher score means a worse outcome.
Time Frame
Up to 1 year after epilepsy surgery
Title
Anxiety assessed by the State-Trait Anxiety Inventory
Description
The State-Trait Anxiety Inventory (STAI) with 40 items, range of scores, 20 to 80. Higher score means a worse outcome.
Time Frame
Up to 1 year after epilepsy surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male or female aged between 18 and 60 years; drug- resistant temporal lobe epilepsy, remaining seizures after two or more tolerated and appropriately chosen antiepileptic drugs; monthly or more seizures during the preceding year prior to trial; the full- scale intelligence quotient (IQ) more than 70, understanding and completing the trial; signing the informed consent; good compliance, at least 12- month follow- up after surgery. Exclusion Criteria: tumor in temporal lobe; extratemporal epilepsy and temporal plus epilepsy; drug- responsive epilepsy, seizure freedom with current drugs in recent one year; pseudoseizures; seizures arising from bilateral temporal lobes; significant comorbidities including progressive neurological disorders, active psychosis, and drug abuse; a full- scale IQ lower than 70, unable to complete tests; previous epilepsy surgery; poor compliance and inadequate follow- up.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yong Liu, MD
Phone
+8618049529896
Email
liu868yong@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Qiang Meng, MD
Phone
+8618092586275
Email
mengqiang2019@xjtu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hua Zhang, PhD
Organizational Affiliation
First Affiliated Hospital Xi'an Jiaotong University
Official's Role
Study Chair
Facility Information:
Facility Name
First Affiliated Hospital of Xi'an Jiaotong University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710061
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hua Zhang, PhD
Phone
008618909225508
Email
zhanghua@xjtu.edu.cn

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is not a plan to make individual participant data (IPD) available to other researchers.
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Minimally Invasive Surgical Epilepsy Trial for Temporal Lobe Epilepsy

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