Cluster headache (CH) is one of the most severe pain accompanied by ipsilateral autonomic symptoms such as lacrimation and conjunctival injection. CH can be categorized into episodic cluster headache (ECH), chronic cluster headache (CCH), and probable CH. Intervention for CH requires a multifaceted and early approach and varies due to the heterogeneity of patients, which makes it difficult to formulate appropriate treatment plan, and the minimally invasive interventional therapy between drug and surgical treatment is still worth looking forward to. The pterygopalatine ganglion, also known as SPG, is a essential proportion in activation of cortical structures and plays an important role in the pathogenesis of CH attacks, which makes it the potential therapeutic target in drug-resistant CH. Percutaneous pulsed radiofrequency (PRF) at SPG is a minimally destructive treatment which shows efficacy, safety, and repeatedly efficacy for refractory CH. PRF is a reliable alternative with few neurological side effects and complications for patients who have not responded to conservative treatment. However, the long term pain relieve is not satisfying. Platelet-rich plasma (PRP) is an autologous blood-derived product of 3 times concentrated platelet above average levels, which contains many growth factors, cytokines, chemokine, and cell-adhesion molecules, therefore function in the activation and synthesis of healing process, tissue proliferation and regeneration. Researches by Michno etc. and Giaccari etc. have proved that PRP combined with PRF therapy may provide more effective outcome than PRF alone in treatment of neuralgia, but whether the combined therapy can improve the efficacy of CH treatment is not clear. ECH occurs in 90% of the CH patients. The investigators assume that PRP combined with PRF acting on SPG might have better therapeutic effect on ECH than PRF alone, by giving combined treatment or PRF therapy alone according to patients willingness, the investigators plan on conducting this prospective trail to compare the clinical efficacy and safety of PRP combined with PRF versus PRF alone.
Study Type
OBSERVATIONAL
Enrollment
242
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China
change in the weekly frequency of cluster headache attacks
The overall mean change from baseline in the weekly frequency of cluster headache attacks across weeks 1 through 3
Time frame: At 1 week, 2 weeks, 3 weeks after the operation
change in the weekly frequency of cluster headache attacks
the overall mean change from baseline in the weekly frequency of cluster headache attacks
Time frame: At 1day, 3days, 1week, 2weeks, 1month, 3months, 6months and 1year after the operation
the percentage of patients with a reduction of at least 50% in the weekly frequency of cluster headache attacks
the percentage of patients with a reduction from baseline of at least 50% in the weekly frequency of cluster headache attacks
Time frame: At 1day, 3days, 1week, 2weeks, 1month, 3months, 6months and 1year after the operation.
the degree of pain
the degree of pain during headache attacks (NRS scores)
Time frame: At 1day, 3days, 1week, 2weeks, 1month, 3months, 6months and 1year after the operation.
the duration of each headache attack
the duration of each headache attack
Time frame: At 1day, 3days, 1week, 2weeks, 3 weeks, 1month, 3months, 6months and 1year after the procedure.
dose of auxiliary analgesic drugs
the dose of auxiliary analgesic drugs taken
Time frame: At 1day, 3days, 1week, 2weeks, 3 weeks, 1month, 3months, 6months and 1year after the procedure.
self-rated patient satisfaction
the self-rated patient satisfaction, from 0 point for unsatisfied to 10 points for very satisfied.
Time frame: At 1day, 3days, 1week, 2weeks, 3 weeks, 1month, 3months, 6months and 1year after the procedure.
WHOQOL-BREF
the degree of patient satisfaction measured by WHOQOL-BREF (World Health Organization Quality of Life Questionnaire).
Time frame: At 1day, 3days, 1week, 2weeks, 3 weeks, 1month, 3months, 6months and 1year after the procedure.
adverse events
For intraoperative AEs, the occurrence of puncture pain, headache, dizziness, nausea, vomiting, facial haematoma and other effects will be recorded. For postoperative AEs, headache, dizziness, facial numbness and other effects will also be recorded.
Time frame: At 1day, 3days, 1week, 2weeks, 3 weeks, 1month, 3months, 6months and 1year after the procedure.
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