Treatment of the knee Anterior Cruciate Ligament Rupture.

Comparison of clinical outcome between Transportal and Transtibial Techniques in Unilateral Primary Anterior Cruciate Ligament Reconstruction of Knee: A single-blind Randomized Clinical Trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016101329132N3

Enrollment

Registered

2016-11-09

Start date

2015-11-10

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior cruciate ligament injury. Sprain and strain involving (anterior)(posterior) cruciate ligament of knee

Interventions

Intervention 1: - Intervention group 1 (trans-tibial group): After standard prepping and draping, the knee was kept in 90 degrees of flexion. At the beginig of surgery, a 3-cm incision is made over pe

Treatment - Surgery

- Intervention group 1 (trans-tibial group): After standard prepping and draping, the knee was kept in 90 degrees of flexion. At the beginig of surgery, a 3-cm incision is made over pes anserinus tend

- Intervention group 2 (trans-portal group): After standard prepping and draping, the knee was kept in 90 degrees of flexion. At the beginig of surgery, a 3-cm incision is made over pes anserinus tend

Eligibility

Sex/Gender

All

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: individuals with anterior cruciate ligament tearing (grade 3) during recent 6 months and inappropriate response to non-surgical treatment. Exclusion criteria: a BMI lower than and greater than 30; previous history of articular surface injury to the same knee joint and previous major surgery in the same knee joint indicated for ligament reconstruction; abnormal renal function tests (blood creatinine more than 1.5 mg/dl or creatinine clearance less than 60); abnormal liver function tests (ALT> 40, AST> 40); known cases of myofascial pain syndromes and fibromyalgia; Patients who did not show up for the follow-up.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
The severity of the pain in knee joint. Timepoint: in the preoperative visit and at 1 month after operation. Method of measurement: Visual Analog Scale (VAS).	—

Secondary

Measure	Time frame
The function of knee joint. Timepoint: in the preoperative visit and at 6 month after operation. Method of measurement: Knee Society Score (KSS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSajad Badiei

Isfahan University of Medical Sciences and Health Services

s_badiei@edc.mui.ac.ir+98 31 3264 4568

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026