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Clinical Randomized Controlled Study on the Comparison of Surgical Treatment and UltrasoundGuided Percutaneous Drainage for Multiple Deep Neck Abscesses

Clinical Randomized Controlled Study on the Comparison of Surgical Treatment and UltrasoundGuided Percutaneous Drainage for Multiple Deep Neck Abscesses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108271
Enrollment
Unknown
Registered
2025-08-27
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Deep Neck Abscess

Interventions

Surgical treatment group:Under general or local anesthesia, an appropriate surgical incision was selected according to the location and extent of the abscess. The abscess was fully exposed, followed b
Ultrasound-guided puncture and drainage group:The patient was placed in an appropriate position and the surgical field was routinely disinfected and draped. Under ultrasound guidance, the location, si

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with multiple deep neck abscesses based on clinical symptoms, signs, laboratory tests (e.g., complete blood count, C-reactive protein), and imaging studies (ultrasound, CT, or MRI), who have not previously received surgical or aspiration drainage treatment; 2. Aged between 18 and 80 years; 3. Patients or their legal guardians who have signed the informed consent form and are willing to comply with all examinations and treatment protocols of this study.

Exclusion criteria

Exclusion criteria: 1. Patients with severe dysfunction of major organs such as heart, liver, or kidney, who cannot tolerate surgery or aspiration drainage; 2. Patients whose abscess has ruptured to the body surface or formed a noticeable sinus tract; 3. Pregnant or breastfeeding women; 4. Patients with coagulation disorders that cannot be corrected to meet the requirements for surgery or aspiration drainage; 5. Patients with a history of neck surgery or radiotherapy that has caused severe local anatomical distortion, potentially affecting the procedure or evaluation of efficacy; 6. Patients with psychiatric disorders who are unable to cooperate with the researchers.

Design outcomes

Primary

MeasureTime frame
success rate of treatment;

Secondary

MeasureTime frame
length of hospital stay;incidence of complications;duration of use of advanced antibiotics;recurrence rate;patient quality of life;

Countries

China

Contacts

Public ContactWenxiang Gao

The First Affiliated Hospital of Sun Yat-sen University

gaowx@mail2.sysu.edu.cn+86 159 1743 5293

Outcome results

None listed

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