Blinding and Data Handling
Cross-source consensus on Blinding and Data Handling from 1 sources and 5 claims.
1 sources · 5 claims
Risks & contraindications
Other
Other
Highlighted claims
- Patients and follow-up personnel are blinded to group allocation. — Liposomal bupivacaine versus standard ropivacaine for pain control in adults receiving continuous supraclavicular brachial plexus blocks for open elbow arthrolysis: study protocol for a randomised controlled non-inferiority clinical trial
- Outcome assessors are separate from anesthesia, intervention delivery, and medication preparation. — Liposomal bupivacaine versus standard ropivacaine for pain control in adults receiving continuous supraclavicular brachial plexus blocks for open elbow arthrolysis: study protocol for a randomised controlled non-inferiority clinical trial
- Data entry and statistical analysis are performed by blinded independent personnel until trial completion and database lock. — Liposomal bupivacaine versus standard ropivacaine for pain control in adults receiving continuous supraclavicular brachial plexus blocks for open elbow arthrolysis: study protocol for a randomised controlled non-inferiority clinical trial
- Unblinding is reserved for severe adverse events such as local anesthetic toxicity. — Liposomal bupivacaine versus standard ropivacaine for pain control in adults receiving continuous supraclavicular brachial plexus blocks for open elbow arthrolysis: study protocol for a randomised controlled non-inferiority clinical trial
- Study data are stored locally and in cloud services with encryption, access controls, backups, recovery mechanisms, cleaning, and multiperson validation. — Liposomal bupivacaine versus standard ropivacaine for pain control in adults receiving continuous supraclavicular brachial plexus blocks for open elbow arthrolysis: study protocol for a randomised controlled non-inferiority clinical trial