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A Clinical Study on Warm Needling Moxibustion at Tianshu and Guanyuan Acupoints

A Clinical Study on Warm Needling Moxibustion at Tianshu and Guanyuan Acupoints

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07483229
Enrollment
60
Registered
2026-03-19
Start date
2022-08-01
Completion date
2025-10-30
Last updated
2026-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Constipation - Functional

Keywords

Yang Deficiency, Warm Needling, Tianshu Acupoint, Guanyuan Acupoint, Traditional Chinese Medicine, Randomized Controlled Trial

Brief summary

This study aims to compare the effectiveness of two different acupuncture techniques for treating a specific type of chronic constipation, known in Traditional Chinese Medicine as "Yang deficiency type" chronic functional constipation. Chronic functional constipation is a common condition characterized by difficult or infrequent bowel movements. The "Yang deficiency" pattern is believed to be caused by a lack of functional energy (Qi) and warmth in the body, leading to sluggish bowel motility. This study will enroll 60 eligible participants who will be randomly assigned to one of two groups: Experimental Group: Participants will receive "warm needling" therapy. This involves inserting acupuncture needles at specific points (Tianshu and Guanyuan) and then burning a small moxa stick on the needle handle to generate heat. Control Group: Participants will receive electroacupuncture at the same acupoints. This involves attaching the needles to a device that delivers a mild electric current. Both groups will receive treatment every other day, three times a week, for a total of four weeks. We will assess their constipation symptoms, anxiety and depression levels, and quality of life using standardized questionnaires immediately after the 4-week treatment and again 6 months later. The goal is to see which method provides better relief, both in the short term and long term.

Detailed description

Background and Rationale Chronic functional constipation (FC) is a highly prevalent disorder that significantly diminishes quality of life and is frequently associated with psychological comorbidities such as anxiety and depression. Within the framework of Traditional Chinese Medicine (TCM), a prominent subtype is "Yang deficiency type" FC. Its pathophysiology is understood as a deficiency of Yang Qi, resulting in slowed metabolism and weakened motility of the large intestine. The acupoints Tianshu (ST25), the Front-Mu point of the Large Intestine, and Guanyuan (CV4), the Front-Mu point of the Small Intestine and a crucial point for nourishing Yuan Qi, are classically combined to warm Yang and regulate intestinal function. This trial investigates whether the combined thermal and stimulatory effects of warm needling at these points offer superior and more sustained clinical benefits compared to electroacupuncture alone. Study Design and Methodology This is a single-center, parallel-group, superiority randomized controlled trial with a 1:1 allocation ratio, conducted at the First Affiliated Hospital of Henan University of Chinese Medicine. A total of 60 participants diagnosed with Yang deficiency type chronic FC will be randomized into either an experimental group (warm needling) or a control group (electroacupuncture). Intervention Details Experimental Group (Warm Needling): After standard disinfection, single-use sterile stainless steel needles (0.25×40mm) will be inserted perpendicularly at Tianshu (ST25) and Guanyuan (CV4) to achieve deqi (the characteristic needling sensation). Subsequently, a prepared moxa stick (approx. 2cm in diameter, 3cm in length) will be attached to the handle of each needle and ignited. The heat is conducted down the needle to the deeper tissues. Needles will be retained for 30 minutes with careful monitoring to prevent burns. Control Group (Electroacupuncture): Needle insertion and deqi technique will be identical to the experimental group. Needle handles will then be connected to an electroacupuncture device (Hwato SDZ-V series) delivering a dense-sparse wave (2/15 Hz) at an intensity sufficient to produce mild, non-painful muscle twitching. Needles will be retained for 30 minutes. Both groups will receive treatment every other day, three times weekly, for a total course of four weeks. Therapeutic Rationale Tianshu (ST25) is strategically selected for its direct regulatory effect on large intestine function. Guanyuan (CV4) is chosen for its powerful action in warming and tonifying Yang Qi. The warm needling technique synergistically combines the meridian-regulating effect of acupuncture with the deep, penetrating warmth of moxibustion. This is hypothesized to enhance local circulation, modulate neuroendocrine pathways involved in the brain-gut axis, and provide a more potent Yang-tonifying effect than electroacupuncture alone, potentially leading to more durable improvements in bowel function. Follow-up and Outcome Assessment To evaluate the sustainability of the treatment effect, all participants will undergo a follow-up assessment six months after the completion of the 4-week treatment course. No study-related interventions will be provided during this period. The primary outcome is the change from baseline in the Constipation Severity Score (CSS) at week 4 and month 6. Secondary outcomes include changes in TCM syndrome score, Self-Rating Anxiety Scale (SAS), Self-Rating Depression Scale (SDS), and Patient Assessment of Constipation Quality of Life (PAC-QOL) scale. Outcome assessors and statisticians will be blinded to group allocation. Analysis will be conducted on an intention-to-treat basis. Significance This study aims to provide rigorous clinical evidence on the efficacy of warm needling for a well-defined TCM condition. By including a 6-month follow-up, it will offer valuable insights into the durability of the therapeutic response, informing clinical practice and guiding future research on non-pharmacological interventions for chronic functional constipation.

Interventions

DEVICEWarm Needling

Warm Needling: After routine disinfection with 75% alcohol, disposable sterile stainless steel acupuncture needles (0.25×40 mm) are inserted perpendicularly at Tianshu (ST25) to a depth of approximately 25 mm and at Guanyuan (CV4) to approximately 20 mm. After achieving deqi (local soreness, distension, or radiation to ipsilateral abdomen or groin), a moxa stick (diameter 2 cm, length 3 cm) is ignited and attached to the needle handle with the lit end facing upward. Needles are retained for 30 minutes per session, with care taken to avoid skin burns. Treatment is administered every other day, three times weekly, for a total of four weeks.

DEVICEElectroacupuncture

Electroacupuncture:After routine disinfection with 75% alcohol, disposable sterile stainless steel acupuncture needles (0.25×40 mm) are inserted perpendicularly at Tianshu (ST25) to a depth of approximately 25 mm and at Guanyuan (CV4) to approximately 20 mm. After achieving deqi (local soreness, distension, or radiation to ipsilateral abdomen or groin), a balanced tonifying and reducing technique is used. The needle handles are connected to an electroacupuncture device (Hwato SDZ-V series electronic needle therapy instrument) with a dense-sparse wave (2/15 Hz) at an intensity sufficient to produce mild muscle twitching. Needles are retained for 30 minutes per session. Treatment is administered every other day, three times weekly, for a total of four weeks.

Sponsors

The First Affiliated Hospital of Henan University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Parallel-group, superiority randomized controlled trial with 1:1 allocation. Participants are randomized to receive either warm needling or electroacupuncture at Tianshu (ST25) and Guanyuan (CV4). Both groups follow the same treatment schedule: every other day, three times weekly for four weeks. Outcome assessors and statisticians are blinded to group allocation; participants and acupuncturists are not blinded due to the nature of the interventions.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Age 18 to 65 years, either sex Meeting the Rome IV diagnostic criteria for functional constipation Meeting the Traditional Chinese Medicine diagnostic criteria for Yang deficiency type constipation No other treatments received before inclusion Exclusion of organic digestive system lesions confirmed by colonoscopy or other appropriate examinations Voluntary participation with signed informed consent

Exclusion criteria

Not meeting the inclusion criteria Pregnant or lactating women Serious cardiovascular or cerebrovascular diseases Inability to receive abdominal acupuncture due to skin diseases or other local conditions Participation in other clinical trials within the past 3 months

Design outcomes

Primary

MeasureTime frameDescription
Constipation Severity Score (CSS)Change from baseline in Constipation Severity Score (CSS) at week 4 and month 6.Change from baseline in Constipation Severity Score (CSS) at week 4 and month 6. CSS (Cleveland Constipation Scoring System) assesses constipation severity; higher scores indicate greater severity.

Secondary

MeasureTime frameDescription
TCM syndrome scoreChange from baseline in TCM syndrome score at week 4 and month 6.A TCM syndrome scoring scale was developed based on the 'Consensus Opinion on the Diagnosis and Treatment of Functional Constipation Using Integrated Traditional Chinese and Western Medicine (2017)'. Primary symptoms were scored 0, 2, 4, 6; secondary symptoms 0, 1, 2, 3.
Self-Rating Anxiety Scale (SAS) scoreChange from baseline in Self-Rating Anxiety Scale (SAS) score at week 4 and month 6.Change from baseline in Self-Rating Anxiety Scale (SAS) score at week 4 and month 6. Higher scores indicate more severe anxiety.
Self-Rating Depression Scale (SDS) scoreChange from baseline in Self-Rating Depression Scale (SDS) score at week 4 and month 6Change from baseline in Self-Rating Depression Scale (SDS) score at week 4 and month 6. Higher scores indicate more severe depression.
Patient Assessment of Constipation Quality of Life (PAC-QOL) scaleChange from baseline in Patient Assessment of Constipation Quality of Life (PAC-QOL) scale at week 4 and month 6Change from baseline in Patient Assessment of Constipation Quality of Life (PAC-QOL) scale at week 4 and month 6. Higher scores indicate worse quality of life.
Clinical efficacyClinical efficacy at week 4Clinical efficacy at week 4, categorized as cured, significantly effective, effective, or ineffective according to the consensus. Total effective rate = (cured+significantly effective+effective)/total×100%.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026