Serratus Plain Block Versus Paravertebral Block Versus Serratus Plain Block and Paravertebral Block for Postoperative Pain Following Thoracoscopic Surgery
- Conditions
- Anesthesia, LocalPain, Postoperative
- Interventions
- Drug: loco-regional anesthesia serratus plane bloc (Ropivacaine 2 mg/mL, 40 mL) and paravertebral placebo bloc (saline, 20 mL)
- Registration Number
- NCT04222010
- Lead Sponsor
- Centre Hospitalier Universitaire, Amiens
- Brief Summary
Acute and chronic postoperative pain remains a major concern following thoracoscopic surgery. Firstly because pain constitutes a serious concern for patients after surgery, and secondarily because an ineffective control of pain may lead to postoperative morbidity, especially in lung cancer surgery.
To date, several procedures have been described but the best modality of locoregional analgesia for thoracoscopic surgery has not been assessed yet. The main objective of this study is to evaluate efficiency of several validated approaches for preoperative locoregional analgesia, comparing serratus plain block versus paravertebral block versus serratus plain block and paravertebral block for postoperative pain following thoracoscopic surgery.
To this end, the investigators will conduct an interventional prospective monocentric, double blind, compared and randomized study. Previously to thoracoscopic surgery, patients will be randomized in one of the three following arms: serratus plain block, paravertebral block or serratus plain block and paravertebral block combined.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 155
- adult patient over18 years old
- without guardianship
- video-assisted thoracoscopic surgery with 3 trocars
- No cons-indications to loco-regional anesthesia (allergy, skin condition)
- patient under 18 years old
- patient under guardianship
- pregnant
- rejection of consent
- rejection of loco-regional anesthesia
- chronic pain antecedents under morphine medication
- pain assessment impossible
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description serratus loco-regional anesthesia loco-regional anesthesia serratus plane bloc (Ropivacaine 2 mg/mL, 40 mL) and paravertebral placebo bloc (saline, 20 mL) patient who underwent thoracoscopic surgery will be assigned to serratus plane bloc (Ropivacaine 2 mg/mL, 40 mL) and paravertebral placebo bloc (saline, 20 mL)
- Primary Outcome Measures
Name Time Method Pain Visual analog scale (VAS) score at coughing Immediately after following thoracoscopic surgery Visual analogue scales (VAS) are 10-cm lines anchored at the ends by words that define the bounds of various pain dimensions. The patient is asked to place a vertical mark on the scale to indicate the level of intensity of his or her pain.
Numerical rating scales are similar to analogue scales except that numbers (e.g., 0 to 5) are entered along the scale.
With category scales, the patient is asked to circle the word that best describes his or her condition (e.g., for pain intensity: None, Moderate, Severe, Unbearable).
- Secondary Outcome Measures
Name Time Method Pain Visual analog scale (VAS) score at coughing Day3 = 3 days following thoracoscopic surgery Visual analogue scales (VAS) are 10-cm lines anchored at the ends by words that define the bounds of various pain dimensions. The patient is asked to place a vertical mark on the scale to indicate the level of intensity of his or her pain.
Numerical rating scales are similar to analogue scales except that numbers (e.g., 0 to 5) are entered along the scale.
With category scales, the patient is asked to circle the word that best describes his or her condition (e.g., for pain intensity: None, Moderate, Severe, Unbearable).
Trial Locations
- Locations (1)
CHU Amiens
🇫🇷Amiens, France