Clinical Evaluation of the Tiaoshen Anti-Cancer Regimen in Treating Psycho-Neurological Symptom Cluster in Ovarian Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-70
SponsorShanghai Municipal Hospital of Traditional Chinese Medicine

About this trial

The academic community generally believes that cancer symptom clusters (CSCs) are not independent diseases, but a group of symptoms that accompany cancer patients. Based on etiology, they can be classified into CSCs related to tumor progression, CSCs related to cancer treatment, or a combination of both. According to symptom manifestations, they can be divided into psychological symptom CSCs, somatic symptom CSCs, and CSCs with coexisting psychological and somatic symptoms. CSCs are universally present during the progression or treatment of cancer. Traditional Chinese medicine (TCM) can leverage its unique characteristics in the intervention of symptom clusters and symptom management. This study is planned to conduct a high-level, prospective, multicenter, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of a TCM regimen for cancer symptom clusters (CSCs), and to simultaneously analyze the characteristics of the population that may benefit most from TCM treatment for CSCs.

Eligibility criteria

Qualifiers

Histologically or cytologically confirmed primary epithelial ovarian cancer

Meet diagnostic criteria for chronic insomnia defined by the Sleep Disorders Group of the Neurology Branch of the Chinese Medical Association: Pittsburgh Sleep Quality Index (PSQI) total score >8 Piper Fatigue Scale total score >4 and Patient Health Questionnaire-9 (PHQ-9) total score >5

Moderate-to-severe symptom severity (average score ≥4 on the MD Anderson Symptom Inventory for Ovarian Cancer [MDASI-OC] subscale assessing sleep disturbance-fatigue-distress-sadness)

Eastern Cooperative Oncology Group Performance Status (ECOG-PS) score 0-2;

Disqualifiers

Patients scheduled to undergo radiotherapy within the next 4 treatment cycles

Comorbid severe primary diseases of the heart, brain, liver, kidney, or hematopoietic system, including hepatic dysfunction (AST/ALT >1.5 times the upper limit of normal [ULN]) or renal impairment (serum creatinine [Cr] >1.2 times ULN)

Pregnant or lactating women, individuals with psychiatric disorders (e.g., schizophrenia, bipolar disorder, mania, depression, anxiety disorders, phobias), intellectual/language impairments, or other mental health conditions;

Scores ≥15 on the Patient Health Questionnaire (PHQ-9) for depression or ≥15 on the Generalized Anxiety Disorder-7 (GAD-7) at screening

Trial design

Treatments tested in this trial

  • Compound Ciwujia Granules
  • Placebo granules
  • Standard treatment protocol for ovarian cancer combined with psychological intervention.

Treatment groups

316 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Shanghai Municipal Hospital of Traditional Chinese Medicine

Lead sponsor

Guangdong Provincial Hospital of Traditional Chinese Medicine

Collaborator

Affiliated Hospital of Qinghai University

Collaborator

Obstetrics & Gynecology Hospital of Fudan University

Collaborator

Fudan University

Collaborator

Beijing Hospital of Traditional Chinese Medicine

Collaborator