Trial Outcomes & Findings for Adductor Canal Block Versus Femoral Block on Pain and Quadriceps Strength (NCT NCT05190120)

NCT ID: NCT05190120

Last Updated: 2025-09-30

Results Overview

Quadriceps strength will be tested with a dynamometer before the nerve block and 20 minutes after the nerve block prior to surgery. The dynamometer measures the strength of the quadriceps muscles in the seated position while pushing against the device. We are trying to measure the effect of both femoral and adductor canal nerve blocks on quadriceps strength.

Recruitment status

COMPLETED

Study phase

PHASE4

Target enrollment

132 participants

Primary outcome timeframe

Baseline and 20 minutes after the block prior to surgery

Results posted on

2025-09-30

Participant Flow

Participant milestones

Participant milestones
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Overall Study
STARTED
31
35
33
33
Overall Study
COMPLETED
25
34
30
27
Overall Study
NOT COMPLETED
6
1
3
6

Reasons for withdrawal

Reasons for withdrawal
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Overall Study
Lost to follow up for primary outcome measurement d/t lack of time to complete before surgery
1
1
1
3
Overall Study
Lost to Follow-up
5
0
2
3

Baseline Characteristics

Adductor Canal Block Versus Femoral Block on Pain and Quadriceps Strength

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
n=26 Participants
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
n=35 Participants
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
n=31 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
n=30 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Total
n=122 Participants
Total of all reporting groups
Age, Continuous
39 years
n=5 Participants
49 years
n=7 Participants
35 years
n=5 Participants
33.5 years
n=4 Participants
36.5 years
n=21 Participants
Sex: Female, Male
Female
8 Participants
n=5 Participants
10 Participants
n=7 Participants
14 Participants
n=5 Participants
14 Participants
n=4 Participants
46 Participants
n=21 Participants
Sex: Female, Male
Male
18 Participants
n=5 Participants
25 Participants
n=7 Participants
17 Participants
n=5 Participants
16 Participants
n=4 Participants
76 Participants
n=21 Participants
Race/Ethnicity, Customized
White
19 Participants
n=5 Participants
21 Participants
n=7 Participants
16 Participants
n=5 Participants
24 Participants
n=4 Participants
80 Participants
n=21 Participants
Race/Ethnicity, Customized
Asian
4 Participants
n=5 Participants
8 Participants
n=7 Participants
10 Participants
n=5 Participants
5 Participants
n=4 Participants
27 Participants
n=21 Participants
Race/Ethnicity, Customized
Black
1 Participants
n=5 Participants
1 Participants
n=7 Participants
0 Participants
n=5 Participants
0 Participants
n=4 Participants
2 Participants
n=21 Participants
Race/Ethnicity, Customized
Hispanic/Latino
2 Participants
n=5 Participants
4 Participants
n=7 Participants
5 Participants
n=5 Participants
1 Participants
n=4 Participants
12 Participants
n=21 Participants
Race/Ethnicity, Customized
Native American or Pacific Islander
0 Participants
n=5 Participants
1 Participants
n=7 Participants
0 Participants
n=5 Participants
0 Participants
n=4 Participants
1 Participants
n=21 Participants
BMI
24.3 kg/m^2
n=5 Participants
28.3 kg/m^2
n=7 Participants
25.4 kg/m^2
n=5 Participants
24.4 kg/m^2
n=4 Participants
25.3 kg/m^2
n=21 Participants

PRIMARY outcome

Timeframe: Baseline and 20 minutes after the block prior to surgery

Population: The participants with data available are reported here.

Quadriceps strength will be tested with a dynamometer before the nerve block and 20 minutes after the nerve block prior to surgery. The dynamometer measures the strength of the quadriceps muscles in the seated position while pushing against the device. We are trying to measure the effect of both femoral and adductor canal nerve blocks on quadriceps strength.

Outcome measures

Outcome measures
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
n=25 Participants
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
n=34 Participants
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
n=27 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
n=24 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Change in Quadriceps Strength Related to the Nerve Block
-0.42 Newtons
Interval -1.2 to 0.23
-0.55 Newtons
Interval -1.43 to -0.067
-3.19 Newtons
Interval -4.25 to -1.73
-0.77 Newtons
Interval -1.63 to 0.0

SECONDARY outcome

Timeframe: worse pain in first 24 hours

Population: The participants with data available are reported here.

As this is an outpatient surgery, we will collect Numerical Pain Scores from the recovery room medical record after surgery as well as from the patients for the first 24 hours after surgery by contacting them at home the following day. We will evaluate the difference in patient pain scores between the two nerve blocks under study. The highest pain score for the 24-hour post-op period was collected for each participant. The median is reported for all participants. A pain score of 10 represents the worst pain.

Outcome measures

Outcome measures
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
n=24 Participants
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
n=32 Participants
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
n=31 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
n=30 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Numerical Pain Score From 0-10
4.5 score on a scale
Interval 3.0 to 6.5
5 score on a scale
Interval 3.0 to 7.0
7 score on a scale
Interval 4.0 to 9.0
6.5 score on a scale
Interval 5.0 to 9.0

SECONDARY outcome

Timeframe: 8 to 24 hours

Population: The participants with data available are reported here.

Patients will be contacted after surgery to determine when the nerve block wore off based on their increase in pain

Outcome measures

Outcome measures
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
n=18 Participants
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
n=25 Participants
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
n=29 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
n=28 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Duration of Nerve Block
678 minutes
Interval 454.0 to 903.0
731 minutes
Interval 566.0 to 896.0
889 minutes
Interval 730.0 to 1048.0
923 minutes
Interval 755.0 to 1091.0

SECONDARY outcome

Timeframe: 2 days

Population: The participants with data available are reported here.

Data on the amount of pain medication consumed for the 1st 24 hours after surgery will be collected based on medications that were administered during surgery, in the recovery room and medications that patients took at home after discharge from the recovery room. All pain medications will be converted to morphine equivalence in milligrams and reported that way. The comparison will be the difference in mg morphine equivalence consumption between the two nerve block groups.

Outcome measures

Outcome measures
Measure
Femoral Block for Knee Arthroscopy/Meniscus Surgery
n=22 Participants
Patients scheduled for knee arthroscopy will have a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery
n=32 Participants
Patients scheduled for knee arthroscopy will have an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Femoral Block for ACL Reconstruction
n=30 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and a femoral nerve block done using 0.5% ropivacaine 20ml before surgery.
Adductor Canal Block for ACL Reconstruction
n=30 Participants
Patients scheduled for ACL reconstruction will have a sciatic nerve block and an adductor canal block done using 0.75% ropivacaine 13.3ml before surgery.
Opioid Consumption Reported at mg of Morphine Equivalence
40 Morphine milligram equivalents (MME)
Interval 30.0 to 60.0
51.25 Morphine milligram equivalents (MME)
Interval 40.0 to 70.0
20 Morphine milligram equivalents (MME)
Interval 10.0 to 40.0
20 Morphine milligram equivalents (MME)
Interval 15.0 to 40.0

Adverse Events

Femoral Block for Knee Arthroscopy/Meniscus Surgery

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Adductor Canal Block for Knee Arthroscopy/Meniscus Surgery

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Femoral Block for ACL Reconstruction

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Adductor Canal Block for ACL Reconstruction

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Pedram Aleshi

University of California San Francisco

Phone: (415) 271-1627

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place