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QH Needle Therapy combined with conventional therapy for lung cancer pain: a randomized controlled trial

QH Needle Therapy combined with conventional therapy for lung cancer pain: a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054197
Enrollment
Unknown
Registered
2021-12-11
Start date
2021-12-20
Completion date
Unknown
Last updated
2022-11-14

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

Conditions

Cancer pain related to lung cancer

Interventions

QH Needle Therapy group:QH Needle Therapy plus usual care

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. An imaging and pathological diagnosis of lung cancer and Estimated survival time > 3 months; 2. Aged 18–80 years, male or female; 3. Suffering from moderate or severe cancer pain (a worst pain score of at least 4 on the Brief Pain Inventory -Short Form in Chinese version) 4. Cognitive ability to provide responses during outcome measurement.

Exclusion criteria

Exclusion criteria: 1. Pain unrelated to cancer or cancer treatment. (medical/arthritic disease that could confound or interfere with evaluation of pain or efficacy); 2. Comorbidities such as serious heart, kidney, or liver disease; 3. Severe mental disorder or drug abuse; 4. Pregnant or breastfeeding women; 5. Contraindications to opioids, such as severe respiratory depression, raised intracranial pressure, paralytic ileus, acute abdomen, chronic obstructive airway disease, pulmonary heart disease, acute asthmatic attack, and hypercapnia; 6. Patients are allergic to opioids, non-steroidal anti-inflammatory drugs(NAIDs) , and alcohol; 7. Severe skin infection, lesions, ulcers, and soars in acupuncture area or severe coagulation disorders due to hepatic diseases, diabetes or other disease; 8. Diagnosed with refractory cancer pain and have indications of interventional therapy; 9. Recently received a palliative radiotherapy, nerve lesion, or interventional treatment; 10. Pain related to an oncologic emergency(Bone fracture or impending fracture of weight-bearing bone, neuroaxial metastases with threatened neural injury, infection, obstructed or perforated viscus).

Design outcomes

Primary

MeasureTime frame
Pain Relief Rates;

Secondary

MeasureTime frame
Pain measurement;Douleur Neuropathique 4 questions;PS(ECOG)score;EORTCQLQ-C30 (The European O-rganization for Reasearch and Treatment of Cancer Quality of Life Questionnare-Core 30);Breakthrough pain;Pain-free interval (time from treatment to pain relief [NRS<2]);Duration of pain relief;Analgesic consumption;

Countries

China

Contacts

Public ContactWang Yingqi

Guangdong Provincial Hospital of Chinese Medicine

wyq950101@126.com+86 13145852973

Outcome results

None listed

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