Skip to content

Efficacy of Pecto-intercostal Fascial Block with Ropivacaine-Dexmedetomidine for Acute Poststernotomy Pain Management in Cardiac Surgery

Efficacy of Pecto-intercostal Fascial Block with Ropivacaine-Dexmedetomidine for Acute Poststernotomy Pain Management in Cardiac Surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081929
Enrollment
Unknown
Registered
2024-03-15
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Valvular heart disease

Interventions

Control group (group C):Bilateral ultrasound-guided bilateral parasternal plane block with a total volume of 40 mL of saline solution
Ropivacaine group (group P) :Bilateral ultrasound-guided bilateral parasternal plane block with a total volume of 40 mL of 0.4% ropivacaine
Ropivacaine-dexmedetomidine group (group PD) :Bilateral ultrasound-guided bilateral parasternal plane block with a total volume of 40 mL of 0.4% ropivacaine with 0.2 µg/kg dexmedetomidine

Sponsors

The People's Hospital of Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 20 to 65 years 2. No gender limitation 3. ASA class ? or ?, and NYHA class ? or ? 4. Normal cognitive 5. Mitral and aortic valve replacement

Exclusion criteria

Exclusion criteria: 1. Malignant tumor 2. Serious infection 3. Preexisting major liver, kidney or lung disease, pulmonary hypertension, or abnormal blood clotting function 4. Cardiac reoperation 5. Chronic pain syndrome 6. Application of chronic anti-inflammatory drugs and opioid drugs 7. Individuals with mental illness who cannot cooperate 8. Blood loss is greater than 50% blood volume 9. Maternal 10. Experimental drug allergy 11. Peripheral neuropathy 12. Immunosuppressive therapy or hormone therapy 13. Refusal to participate

Design outcomes

Primary

MeasureTime frame
Dosage of analgesics used during operation and 24h after operation;VAS scores;Bruggrmann comfort scale;

Secondary

MeasureTime frame
PCA bolus;Rapid rehabilitation indicators;Ramsay scores;Duration of nerve block;Adverse reaction indicators;

Countries

China

Contacts

Public ContactLi Yanru

The People's Hospital of Guangxi Zhuang Autonomous Region

dryanru@126.com+86 189 7891 9541

Outcome results

None listed

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