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Non operative cost-effective management of Flatfoot in indian population

Management of posterior tibial tendon dysfunction induced flexible Adult Acquired Flatfoot Deformity-A cost effective conservative management solution for indian population

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029357
Enrollment
170
Registered
2020-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: orthosis Application exercise Regime: patients are given two types of orthosis, that is Prefabricated and custom made orthosis, which is to be worn for certain period and the exercise t

Sponsors

Kasturba medical college HospitalManipal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 35-70 years. 2.Current complaints of pain in the ankle and foot at least for period of 3 months or more. 3.On clinical examination flexible plano-valgus deformity 4.PTTD of stage I or stage II according to Johnson and storm 5. Radiological assessment with longitudinal arch flattening Lateral view:Lateral Talo-first metatarsal angle- >10 degrees Antero-posterior view: Anteroposterior Talo-first metatarsal angle- >10 degree

Exclusion criteria

Exclusion criteria: 1.Rigid foot deformity 2.PTTD of stage III and IV according to Johnson and storm 3. Patients with preexisting fixed foot deformities 4.Previous history of surgery on the same ankle and foot 5.Presence of neurovascular, peripheral vascular, musculoskeletal abnormality

Design outcomes

Primary

MeasureTime frame
Reduction of pain,swelling and deformity of the foot and ankle by Conservative Management with a cost effective custom-made Orthosis combined with Exercise regime. Timepoint: After initial recruitment of Participant First 3 weeks of intervention phase first review at 6 weeks next review at 3 months last review at 6 months. At 6 months review if the patient improves, then review at every 6 months for 4 years. If at 6 months review,,patients condition is status-co or worsens then, patient goes out(excluded) of the study and alternative surgical option offered.

Secondary

MeasureTime frame
improvement in quality of life and cease the progression of the diseaseTimepoint: After initial recruitment of Participant First 3 weeks of intervention phase first review at 6 weeks next review at 3 months last review at 6 months. At 6 months review if the patient improves, then review at every 6 months for 4 years. If at 6 months review,,patients condition is status-co or worsens then, patient goes out(excluded) of the study and alternative surgical option offered.

Countries

India

Contacts

Public ContactKrishnaprasad P R

Kasturba Medical college,Manipal, MAHE(Manipal Academy of Higher Education)University

krishna.ppr@manipal.edu9845045970

Outcome results

None listed

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