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Trial · NCT02593370

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBlock successEstimated 40 min after completed intervention. Presented 10 months after last patient last visit (LVLP).
Block success of the clinical relevant lumbosacral nerves that innervate the hip joint capsule estimated as significant motor block of the obturator nerve, the femoral nerve, and the lumbosacral trunk. Motor block is a significant proxy marker of sensory block. Motor block (muscle strength, mmHg) is assessed with a handheld dynamometer.
SecondaryPlasma lidocaineBlood samples are withdrawn 0, 5, 10, 20, 40, 60, and 90 minutes after intervention. Presented 10 months after LVLP
SecondaryTime for preparationEstimated prior to intervention. Presented 10 months after LVLPTime for preparation in seconds is defined as the time of placement of the volunteer on the bed until the end of pre-ultrasound scanning
SecondaryBlock procedure timeEstimated during intervention. Presented 10 months after LVLPBlock procedure time in seconds is defined as the time of the placement of the ultrasound probe on the skin to until the block needle is pulled out after injection of local anesthetics
SecondaryInjection siteEstimated at the end of the intervention. Presented 10 months after LVLP
SecondaryBlock needle depthEstimated at the end of the intervention. Presented 10 months after LVLP
SecondaryDiscomfortEstimated immediately after the intervention. Presented 10 months after LVLPEstimated on numeric rating scale 0-10
SecondaryMean arterial pressure changeMean arterial pressure is measured prior intervention and 5 min after intervention. Presented 10 months after LVLP
SecondarySensory (cold, warm, touch, pain) block of the dermatomes T12-S3 and the lateral femoral cutaneous nerveEstimated 50 min after intervention. Presented 10 months after LVLP
SecondaryPerineural spread of local anesthetics added gadoterate meglumineEstimated on MRI sampled 10-30 minutes after intervention. Presented 10 months after LVLP
SecondaryEpidural spread of local anesthetics added gadoterate meglumineEstimated on MRI sampled 10-30 minutes after intervention. Presented 10 months after LVLP
SecondaryCost-effectiveness (ICER)Calculated after LVLP. Presented 10 months after the last visit of the last volunteerICER is estimated as the difference in mean marginal cost of the blocks.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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