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Effect of Additional Lumbosacral Brace on the Outcome of Patients with Acute Low Back Pain at the Aga Khan University Hospital, Nairobi

Effect of Additional Lumbosacral Brace on the Outcome of Patients with Acute Low Back Pain at the Aga Khan University Hospital, Nairobi

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201508000907314
Enrollment
82
Registered
2014-10-08
Start date
2013-03-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Musculoskeletal Diseases low back pain Anaesthesia

Interventions

standard analgesic protocol
Lumbosacral Corset in addition to the standard analgesia protocol

Sponsors

Aga Khan Unviersity Hospital, Research Office
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ¿ Acute low back pain patients aged 18-60 years. An episode of acute low back pain is defined as pain bound by 12th rib superiorly, gluteal creases inferiorly without leg pain, occurring over a duration of up to 6 weeks (van tulder-european guidelines, de vet ¿definitions) ¿ Consenting

Exclusion criteria

Exclusion criteria: ¿ Red flags (indicators of serous pathology as picked from history and physical examination) o age less than 15 or more than 60 years o history of trauma or injury to the back o thoracic spine pain o past history of cancer o prolonged use of steroids o unexplained weight loss o symptoms of cord compression with focal deficits (saddle anaesthesia, limb weakness, urine incontinence or retention, cauda equina syndrome) o structural deformity of the back o fever and signs of infection - present or past (urinary infection, TB) ¿ Those who have used a lumbar corset before ¿ Patient who have already used the analgesics before ¿ Patients who have had spine surgery. ¿ Patients suffering from heart or respiratory disease ¿ Pregnant patients ¿ Patients already on the analgesic protocol with worsening pain

Design outcomes

Primary

MeasureTime frame
back specific disability as measured on the Oswestry disability Index

Secondary

MeasureTime frame
change in Pain score as measured through visual analogue score (VAS) f

Countries

Kenya

Contacts

Public Contactaruyaru Mwenda

principal research

arumwesta@gmail.com+254720921267

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026