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NCT01505374 · ClinicalTrials.gov registry record · NA

Saphenous Nerve Block vs. Femoral Nerve Block for Total Knee Arthroplasty

A NA study of Difference Between Femoral Nerve Block and Saphenous Block, sponsored by Hospital for Special Surgery, New York.

Completed
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT01505374: Completed NA study of Difference Between Femoral Nerve Block and Saphenous Block, sponsored by Hospital for Special Surgery, New York.

NCT01505374 is a NA study of Difference Between Femoral Nerve Block and Saphenous Block that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01505374, a NA study of Difference Between Femoral Nerve Block and Saphenous Block, has completed, sponsored by Hospital for Special Surgery, New York.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

Currently, the regional anesthetic standard of care for total knee replacement surgery is combined spinal/epidural to provide long-lasting pain relief with or without a femoral nerve block (FNB). The femoral nerve block refers to a technique that your anesthesiologist can use to numb the thigh muscle for approximately 18 hours after surgery. While this technique offers significant pain relief, it is possible it may cause muscle weakness and increase patients' recovery times. Hence there is a need for an alterative anesthetic technique, one that may help minimize postoperative pain as effectively as a femoral nerve block, while not causing weakness of the thigh muscle. The saphenous nerve, a branch of the femoral nerve, provides sensation to the knee. Thus it is hypothesized by "blocking" or anesthetizing the saphenous nerve with local anesthetic closer to where it branches off, the area around and below the knee will feel numb. Yet unlike the femoral nerve block, the thigh muscle itself will still be able to function. For patients undergoing two total knee replacements at one time or bilateral total knee replacement, they will be randomly assigned to receive a femoral nerve block on one leg and a saphenous block on the other. Pain levels will be measured and thigh muscle strength will be tested using a dynamometer before surgery, 6-8 hours following anesthesia administration, and on postoperative days 1 and 2.

Primary Outcome

The primary outcome is the postoperative pain in each leg within the first 24 hours postoperatively. VAS pain scores could range from 0 to 10. Higher values represent a worse outcome.

Interventions

  • PROCEDURE Study Technique
  • PROCEDURE Control Technique

Study Locations (1)

New York

  • Hospital for Special Surgery - New York

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2012-03
Est. Completion 2013-09
Phase NA

What the finished NCT01505374 record still lists

NCT01505374 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Difference Between Femoral Nerve Block and Saphenous Block appearing as the primary indexed condition, and to 2 interventions - of which Study Technique is the first listed.

NCT01505374 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT01505374 about?

NCT01505374 is a clinical study titled "Saphenous Nerve Block vs. Femoral Nerve Block for Total Knee Arthroplasty". Currently, the regional anesthetic standard of care for total knee replacement surgery is combined spinal/epidural to provide long-lasting pain relief with or without a femoral nerve block (FNB). The femoral nerve block refers to a technique that your anesthesiologist can use to numb the thigh muscl...

What is the current status of trial NCT01505374?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2012-03. Estimated completion is 2013-09.

What conditions does trial NCT01505374 study?

This clinical trial studies the following conditions: Difference Between Femoral Nerve Block and Saphenous Block.

What interventions are being tested in trial NCT01505374?

The interventions under investigation include: Study Technique (PROCEDURE), Control Technique (PROCEDURE).

Who is sponsoring clinical trial NCT01505374?

This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01505374 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT01505374's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01505374, the US trial registry maintained by the National Library of Medicine. NCT01505374 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.