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Active, Not Recruiting

NCT Number: NCT04198181

The Effectiveness and Safety of Resective Epilepsy Surgery for TRE

A prospective cohort studies to identify clinical seizure control, cognitive changes, and safety in resective epilepsy surgery in patients with TSC-related drug-resistant epilepsy.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

Two hundred candidates are recruited and assigned to the control and surgery groups with 100 cases in each group, respectively. All patients will accept first-stage pre-enrollment evaluations and patients in surgery group will accept second-stage invasive evaluation.

All patients will be advised to visit the hospitals for examination each year after enrollment. Seizure outcomes will be assessed with reference to patients' seizure diaries and caregivers' oral statements by both neurosurgeons and neurologists.

All adverse effects will be classified according to the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0 (2017).

Statistical analyses were conducted using SPSS (version 26.0, IBM, USA), Stata (version 16.0, Stata Corp LLC, USA), and R (version 4.3.3, R Foundation for Statistical Computing, Austria). Outcomes were presented according to data type as percentages, mean ± standard deviation, or median (interquartile range, IQR).

Multiple imputation was employed to address missing data for IQ and QOL at enrollment and the 2-year follow-up. A sensitivity analysis was conducted to assess the robustness of the multiple imputation results. The "mi impute regress" statement in Stata facilitated the multiple imputations. 20 T-tests were utilized for comparing continuous variables, with results reported as mean ± standard deviation. The Mann-Whitney U test was applied for non-normally distributed continuous variables, presenting results as median values and IQRs. Chi-square and Fisher's exact tests were used for univariate analyses. A significance level of p < 0.05 was established.

To account for differences in covariates between the surgery and medicine groups, propensity score matching (PSM) was performed. Based on PSM, Kaplan-Meier curves and the log-rank test were utilized to analyze time-to-seizure recurrence differences between the surgery and medicine groups. Additionally, multivariable Cox proportional hazards regression was applied to predict risk factors for postoperative seizure recurrence within a 51-month follow-up period after PSM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 2 years old and above, no gender restriction, TSC gene monitoring with or without abnormality
  • Diagnosis of tuberous sclerosis- related drug-resistant epilepsy
  • Epilepsy course for more than 1 year
  • Patients who have taken 3 or more reasonable choices with appropriate and tolerable antiepileptic drugs (excluding mTOR inhibitors and traditional Chinese medicine and prescriptions) had seizures more than 12 times in the 3 months before enrollment
  • The family members agreed to enroll and signed the informed consent.

Exclusion criteria

  • Obvious renal angiomyolipoma, pulmonary lymphoma leiomyomatosis, and subventricular giant cell astrocytoma
  • Abnormal heart, lung, liver, and kidney functions and coagulation function
  • Preoperative evaluation, it is considered that no surgical treatment is needed
  • The patient received other craniocerebral surgical treatment within 1 year during the follow-up period

Treatment and study plan

Surgery

Procedure

Resective surgery included lobectomy (partial or total brain lobe resection), tuberectomy (epileptogenic tuber resection), and tuberectomy plus (resection of epileptogenic tuber and perituberal gyri). Tuberectomy was typically performed on the epileptogenic tuber within or near an eloquent area. Lobectomy was performed in patients with large epileptogenic tubers in the brain lobes. Multiple lobectomies, tuberectomies, tuberectomies plus, and lobectomy combined with tuberectomy/tuberectomies plus were further performed in patients with multiple epileptogenic tubers.

Primary outcomes

  1. % of patients with ILAE grading

    Time frame: 3 years

    The grading made by ILAE for the classification of outcome with respect to epileptic seizures following epilepsy surgery. It contains a total of 6 levels. The higher the level, the worse the result. We will count the percentage of patients at each level.

Secondary outcomes

  1. IQ

    Time frame: 3 years

    Wechsler Preschool and Primary Scale of Intelligence(WPPSI-III),Wechsler Intelligence Scale for Children (WISC-IV) and Wechsler Adult Intelligence Scale (WAIS-IV),3 scales will be used for different ages to measure IQ. Higher scores mean better outcomes.

  2. Quality of Life: QOLIE-31

    Time frame: 3 years

    QOLIE-31 is suitable for patients 14 years and older. QOLCE-76 is applied to patients aged 2-13 by parents.

Sponsors and collaborators

Lead sponsor

Beijing Children's Hospital

Other

Collaborators

  • Beijing Sanbo Brain Hospital
  • First Affiliated Hospital Xi'an Jiaotong University
  • Fourth Medical Center of PLA General Hospital
  • Guangdong 999 Brain Hospital
  • Henan Provincial People's Hospital
  • Nanjing Medical University
  • Peking University People's Hospital
  • Ruijin Hospital
  • Shandong Provincial Hospital
  • Shanghai Children's Hospital
  • Shenzhen Children's Hospital
  • The First Affiliated Hospital of Shanxi Medical University
  • The First Affiliated Hospital of University of Science and Technology of China
  • The First Hospital of Jilin University
  • The First Medical Center of Chinese PLA General Hospital
  • The Second Hospital of Hebei Medical University
  • Tiantan Hospital, Capital Medical University
  • West China Hospital
  • Xiangya Hospital of Central South University
  • Xinqiao Hospital, Amry Medical University
  • Xuanwu Hospital, Beijing

Registry information

Official study title

Clinical Evaluation of the Effectiveness and Safety of Resective Epilepsy Surgery for Tuberous Sclerosis Complex Related Epilepsy

Important dates

Study start
2019
Primary completion
2027
Study completion
2027
First posted
Dec 13, 2019
Registry last updated
Jan 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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