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Clinical study on the treatment of renal colic with Qiu acupoint acupressure, an appropriate technique of traditional Chinese medicine

Clinical study on the treatment of renal colic with Qiu acupoint acupressure, an appropriate technique of traditional Chinese medicine

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047168
Enrollment
Unknown
Registered
2021-06-09
Start date
2021-06-20
Completion date
Unknown
Last updated
2022-01-24

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

Conditions

Renal colic

Interventions

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Consistent with the following symptoms and signs: (1) Sudden onset of abdominal pain and discomfort; (2) When the attack physical examination of the affected side of the kidney area may have tenderness or percussion pain; (3) The pain may be accompanied by pallor, weakness, nausea and vomiting, sweating, etc.; (4) Digestive tract reaction (nausea and vomiting, dry mouth); (5) Perineal radiating pain; (6) Urinary irritation symptoms (frequency, urgency and pain); (7) Anorectal stimulation (frequent bowel movement, tenesmus); (8) Today hematuria (mirror or naked eyes), often after the activity; Above symptom (1), (2)is necessary condition; 2. Exclude other symptoms of lumbago that are not caused by ureterospasm; 3. The patient is conscious and has stable vital signs, and can cooperate with the treatment; 4. Voluntarily participate in this clinical trial, give informed consent and sign informed consent; 5. The patient is between 18 and 65 years old.

Exclusion criteria

Exclusion criteria: 1. Delirious, mentally ill, with other serious diseases, unable to cooperate with the treatment of the patient; 2. Women during pregnancy, pregnancy and lactation; 3. Local skin is broken or ulcerated;, with severe primary diseases of viscera and other systems, and with severe urinary tract infection in urgent need of anti-infection treatment; 4. Allergy to non-steroidal anti-inflammatory drugs, previous history of gastrointestinal bleeding or active gastric ulcer, and relevant contraindications prohibited in the drug instructions; 5. Oral history of taking calcium ion blocker and alpha blocker within 4 days before enrollment; 6. Patients with poor treatment compliance; 7. Previous patients with severe cardiovascular and cerebrovascular diseases.

Design outcomes

Primary

MeasureTime frame
Onset time of analgesia;

Secondary

MeasureTime frame
VAS scores at 1, 5, 10, 20, 30 and 120min before and after treatment;Efficiency;The recurrence rate;

Countries

China

Contacts

Public ContactChen Chiwei

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

william_chen1118@126.com+86 13660274305

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026