Acupuncture Reduces Relapse in Patients With Crohn's Disease: a Superiority Trial
NCT06553053 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 106
Last updated 2026-04-13
Summary
The aim of this study was to further improve the clinical efficacy of acupuncture in delaying the clinical recurrence of CD and to explore the efficacy mechanism of acupuncture efficacy enhancement.
Conditions
- Crohn's Disease Relapse
- Inflammatory Bowel Diseases
Interventions
- OTHER
-
"Harmonizing Shaoyang, nourishing spleen and kidney with warmth" Acupuncture Group
Patients receiving acupuncture and mild moxibustion, whom were treated 2 times per week for 12 weeks and followed up for 40 weeks. The first group of acupoints is that CV4 and Bilateral ST37, SP6, SP4, KI3, LI11, SJ4 and GB26 were selected for acupuncture and CV12 and bilateral ST36 and GB41 were selected for moxibustion. The second group of acupoints is that CV12 and Bilateral ST36, GB41, SP4, KI3, LI11, SJ4 and GB26 were selected for acupuncture and CV4 and bilateral SP6 and GB34 were selected for moxibustion. These two groups are alternate. After deqi sensation was even reinforcing and reducing. The surface temperature of acupoints was maintained at 43℃± 1℃ for moxibustion. During each treatment, acupuncture and mild moxibustion are performed simultaneously, both lasting for 30 minutes.
- OTHER
-
"Nourishing spleen and kidney with warmth" Acupuncture Group
Patients receiving acupuncture and mild moxibustion, whom were treated 2 times per week for 12 weeks and followed up for 40 weeks. The first group of acupoints is that CV4 and Bilateral ST37, SP6, SP4, KI3 and LI11 were selected for acupuncture and CV12 and bilateral ST36 were selected for moxibustion. The second group of acupoints is that CV12 and Bilateral ST36, SP4, KI3 and LI11 were selected for acupuncture and CV4 and bilateral SP6 were selected for moxibustion. These two groups are alternate. After deqi sensation was even reinforcing and reducing. The surface temperature of acupoints was maintained at 43℃± 1℃ for moxibustion. During each treatment, acupuncture and mild moxibustion are performed simultaneously, both lasting for 30 minutes.
Sponsors & Collaborators
-
Ruijin Hospital
collaborator OTHER -
Shanghai Institute of Acupuncture, Moxibustion and Meridian
lead OTHER
Principal Investigators
-
Bao Chunhui, MD, PhD · Shanghai University of TCM
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 16 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-13
- Primary Completion
- 2028-12-31
- Completion
- 2028-12-31
Countries
- China
Study Locations
More Related Trials
-
Efficacy of Acupuncture and Moxibustion Treatment in Patients With Active Crohn's Disease
NCT01697761 ·Status: COMPLETED ·Phase: NA
-
Effect of Acupuncture on the Microbiota-gut-brain Axis in Crohn's Disease
NCT06364722 ·Status: COMPLETED ·Phase: NA
-
Efficacy Classification Prediction of the Effects of Acupuncture on Abdominal Pain in Patients With Crohn's Disease
NCT06352164 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Acupuncture and Moxibustion Treatment in Patients With Quiescent Crohn's Disease:Evaluation With fMRI
NCT01696838 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Ustekinumab Therapy in Patients With Symptomatic Stricturing Crohn's Disease
NCT05387031 ·Status: RECRUITING
-
An Observational Study to Assess Change in Disease Activity and Adverse Events in Adolescent and Adult Participants With Moderate to Severe Active Crohn's Disease (CD) in Japan
NCT06023030 ·Status: RECRUITING
-
Impact of Exclusive Enteral Nutrition Therapy on Sperm Quality of Patients With Crohn's Disease
NCT02233062 ·Status: COMPLETED ·Phase: NA
-
Induced Adult Refractory Active Crohn's Disease Clinical Relieving by Using Thalidomide
NCT02956538 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Efficacy of Exclusive Enteral Nutrition in Adult Active Crohn's Disease
NCT05815355 ·Status: COMPLETED
-
Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of Clinical Remission in Subjects With Crohn's Disease
NCT00105300 ·Status: COMPLETED ·Phase: PHASE3
-
Biologics for Stricturing Crohn's Diseases
NCT05645055 ·Status: RECRUITING
-
Upadacitinib for Refractory IBD in Asian Children and Elderly: Age-Stratified Analysis
NCT06922331 ·Status: COMPLETED
-
Nutritional Status and Body Composition of Adult Patients With Crohn's Disease
NCT04915911 ·Status: UNKNOWN
-
Study of Factors and Mechanisms Influencing the Effects of Treatments in Crohn's Disease
NCT04135027 ·Status: UNKNOWN
-
Study to Evaluate the Safety and Efficacy of Adalimumab in Chinese Subjects With Moderate to Severe Crohn's Disease
NCT02499783 ·Status: COMPLETED ·Phase: PHASE3
-
Microflora and Metabolomics of Crohn's Disease Patients
NCT04965584 ·Status: UNKNOWN
-
Active Surgical Intervention on Crohn's Disease
NCT05523050 ·Status: UNKNOWN ·Phase: NA
-
Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Two Treatment Modules in Chinese Subjects With Moderate to Severe Crohn's Disease
NCT02015793 ·Status: COMPLETED ·Phase: PHASE2
-
Therapeutic Optimization Study Based on MR Enterocolonography in Patients With Crohn's Disease
NCT02332356 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Exclusive Enteral Nutrition vs. Infliximab in Chinese CD Patients
NCT04530877 ·Status: WITHDRAWN ·Phase: PHASE4
-
The Effect of Exclusion Diet for Crohn's Disease Plus Enteral Nutrition on Children and Adolescents With Crohn's Disease
NCT06353633 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
IUS Predicts Upadacitinib Efficacy in Patients With Moderate to Severe Crohn's Disease:a Prospective Study
NCT06573944 ·Status: RECRUITING
-
A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical Remission in Subjects With Crohn's Disease
NCT00055523 ·Status: COMPLETED ·Phase: PHASE2
-
HLADQA1*05 Genotype and the Efficacy of Treatment With Infliximab in Chinese Population Crohn's Disease
NCT05813860 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Mesenchymal Stem Cell Therapy for the Treatment of Severe or Refractory Inflammatory and/or Autoimmune Disorders
NCT01540292 ·Status: TERMINATED ·Phase: PHASE1/PHASE2