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临床试验/CTRI/2025/08/092843
CTRI/2025/08/092843尚未招募不适用

Comparative Efficacy of Different Basti Techniques within the kala Basti pattern in low Back pian: An Analytical Cross-sectional Study

National Institute of Ayurveda De Novo1 个研究点 分布在 1 个国家目标入组 280 人开始时间: 2025年8月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
280
试验地点
1
主要终点
Improvement in Oswestry Low Back Disability Questionnaire, The Quebec Back Pain Disability Scale

研究概览

简要总结

Primary purpose of protocol: To determine the relative

effectiveness of various Basti formulations within the Kala

Basti pattern for reducing Low Back Pain (LBP). Additionally,

the study aims to assess the influence of Basti therapy on

outcomes measured by the Oswestry Low Back Disability

Questionnaire, The Quebec Back Pain Disability Scale, and

SF-36 among individuals with LBP.

The methodology of this study involves a comparative analysis

of different Basti formulations within the Kala Basti pattern for

managing Low Back Pain (LBP). Participants will be recruited

and grouped based on specific Basti techniques administered.

Data on pain intensity, functional disability, and quality of life

will be collected using validated scales such as the Oswestry

Low Back Disability Questionnaire, The Quebec Back Pain

Disability Scale, and SF-36. Statistical analyses will be

employed to compare the effectiveness of Basti formulations

and assess their impact on LBP outcomes. Additionally,

subgroup analyses may be conducted to explore the influence

of potential confounding factors.

Dissemination of findings: The findings of the study will be

disseminated through peer-reviewed publications, conference

presentations, and knowledge-sharing platforms within the

Ayurvedic community to inform practice, policy, and future

research endeavors.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 18 to 60 years Patients presenting with a primary complaint of Low Back Pain (LBP) Patients with a confirmed diagnosis of LBP based on clinical evaluation and/or imaging studies Patients scheduled to undergo Basti therapy within the Kala Basti pattern as part of their treatment regimen Patients willing to provide informed consent for participation in the study.

排除标准

  • Patients with contraindications to Basti therapy Patients with a history of significant spinal pathology (vertebral fractures, spinal tumors), severe systemic illness, active infection, or uncontrolled bleeding disorders Patients with a history of adverse reactions or hypersensitivity to the substances commonly used in Basti formulations.

结局指标

主要结局

Improvement in Oswestry Low Back Disability Questionnaire, The Quebec Back Pain Disability Scale

时间窗: Base line and 16th day

次要结局

  • Quality of life - SF 36(Base line & 16th day)

研究者

发起方
National Institute of Ayurveda De Novo
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Prof Gopesh Mangal

National Institute of Ayurveda (De Novo) Jaipur

研究点 (1)

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