Skip to content

Clinical research on the effectiveness and safety of STORZ power system in the surgery of Dowager Hump (Kyphosis)

Clinical research on the effectiveness and safety of STORZ power system in the surgery of Dowager Hump (Kyphosis)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110670
Enrollment
Unknown
Registered
2025-10-17
Start date
2025-10-20
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Dowager Hump (Kyphosis)

Interventions

Experimental group:The dowager hump (kyphosis) operation was performed using the STORZ power system as the experimental equipment.
Control group:The cases of the conventional clinical procedure of aspiration combined with excision of the dowager hump (kyphosis) (including a 6-month follow-up) and the concurrent conventional clini

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Dowager hump (kyphosis) patients who need and are willing to undergo the "" surgery should have a maximum diameter of the "" of >= 8 cm and less than 12 cm. 2. Age should be >= 18 years old and <= 65 years old, and there is no gender restriction. 3.Voluntary participation in this clinical trial and signing the informed consent form, as well as cooperation in follow-up and treatment. 4.Patients who undergo preoperative X-ray, color ultrasound or magnetic resonance imaging (MRI) examination and are clinically diagnosed with "". 5.Have not received recent treatment for "" (such as no physical or drug intervention within 3 months).

Exclusion criteria

Exclusion criteria: 1.Abnormal coagulation function; 2. Compression of the spinal cord, vertebral fractures, and spinal canal stenosis of >=50% or accompanied by severe liver and kidney dysfunction, local infection, other intolerable diseases, etc.; 3. Suffering from mental disorders and unable to cooperate; 4. Pregnant women or having other systemic diseases (severe cardiovascular diseases, hypertension, diabetes, etc.); 5. Subjects considered by the researchers as not suitable for this study; 6. Having a history of neck surgery in the past year and participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Neck and head angle;

Secondary

MeasureTime frame
Length of the incision during the operation;Duration of surgical procedure;Duration of removing the drainage tube after surgery;Vancouver Scar Scale;Associated symptoms improvement: flap necrosis, hematoma/seroma, infection, etc.;

Countries

China

Contacts

Public ContactDamao Dai

Shenzhen People’s Hospital (The First Affiliated Hospital, Southern University of Science and Technology;The Second Clinical Medical College,Jinan University)

handsomeddm@163.com+86 137 6329 4227

Outcome results

None listed

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