- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05641038
Comparison Of The Efficiencies Of Peloid and Paraffine Treatments In Patients With Hallux Rigidus
Comparison Of The Efficiencies Of Peloid Therapy and Paraffine Treatments In Patients With Hallux Rigidus
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hallux rigidus(HR); It is a pathology seen in the first Metatarsophalangeal (MTF) joint, characterized by pain, dorsal osteophytes, and dorsiflexion difficulties due to progressive degenerative arthritis. (1) The most common deformity of the first MTF joint is hallux valgus, and the second most common deformity is HR. Its incidence is higher in women than in men.(2, 3) Clinically, HR typically has insidious onset pain in the MTF joint when walking and a decrease in joint range of motion (ROM).(4) X-rays are used in radiological evaluation; narrowing of the joint space, osteophytes in the head of the metatarsal and proximal phalanx, and deterioration of the nonuniform cartilage can be observed. (5) The Coughlin and Shurnas staging system, which was created in 1999 by adding range of motion and patient's symptoms to radiological findings, is one of the most preferred.(6) This staging system was used in the staging of the patients in our study.
Treatment of HR varies according to the patient's clinic and the stage of the disease. The preferred treatment option in the early period is conservative methods. Nonsteroidal anti-inflammatory drugs (NSAI) can be used to alleviate synovitis and joint inflammation. (7) Other non-operative treatment modalities of HR include physical therapy modalities (hot-cold therapy, electrotherapy), exercise (stretching-strengthening exercises), bracing, manipulation. ..etc.(8,9) However, hard-soled shoes with a deep and wide front are recommended for activity modification and reduction of dorsal compression. Dynamic splinting can be applied to patients to increase dorsiflexion. (10) Intra-articular steroid, hyaluronic acid or platelet rich plasma (PRP) injection can be applied to patients who do not respond to these treatments. (8,11) There are many surgical methods defined for the treatment of HR. These; joint debridement, osteophyte excision, resection arthroplasty, interposition arthroplasty, cheilectomy, proximal phalangeal or metatarsal osteotomy, arthrodesis and implant arthroplasty.(12) Paraffin therapy is one of the superficial heating treatment methods. The melting point of solid paraffin is 70-80 degree. This temperature is reduced to 50-55 degree by adding 1/4 - 1/7 liquid paraffin or mineral oil. (13) There are two application methods, immersion and brushing. The immersion method is applied to the extremities, that is, for the hands, feet and arms. Brushing method is more suitable for other parts of the body such as hips, shoulders and back. With paraffin treatment, a very intense heat transfer is provided to the body. It is known that paraffin therapy also creates an increase in temperature in the joint capsule and muscles. (14) Peloids are mixtures of organic and/or inorganic substances formed as a result of biological, climatological and/or geological events. Peloid therapy is a special balneotherapy method made with natural mud.(15,16) Peloids can be applied in the form of baths (full, half, sitting and extremity baths), packs, tampons, kneading and masks. The most commonly used method in peloid therapy is packaged applications. (17) They provide relief of muscle spasm and reduction of pain with their mechanical effects. In the venous system, blood is directed towards the heart from the peripheral veins. There is a decrease in peripheral vein tone, a decrease in diastolic pressure, and a slight increase in systolic blood pressure. Vasodilation occurs in the relevant deep parts of the body with the cutaneous reflex that arises with stimulation in the parts of the body that come into contact with the peloid, muscle spasm, which is mostly thought to be due to ischemia, is resolved by thermic effect and vasodilation, vasodilation helps to clear the metabolic wastes that may cause pain from the tissue and as a result, the pain disappears. It causes relaxation in muscles, soft tissues (such as tendons, ligaments, fascia and joint capsule), raises the pain threshold at nerve endings and provokes a series of neuroendocrine reactions. In addition, hot applications have an anti-inflammatory effect in chronic inflammations. (16,18) The organic (bitumen, pectin, cellulose, lignin, humin, sulfoglycolipids, humic, fulvic and ulmic acids) and inorganic (sulphur, sodium and magnesium chloride, sulfate, iodine, bromine, zinc and selenium) substances contained in the peloid also cause many effects in the body. . The absorption of these substances through the skin causes vasodilation, relaxation in smooth muscles, inhibition of inflammation in Langerhans cells in the skin, stopping the breakdown of arachidonic acid into prostaglandins, suppressing hyaluronidase activity, and antioxidant, antiviral and anti-inflammatory effects.(19,20) Thermal mud baths activate the pathway. It has been shown to cause an increase in various hormones, a decrease in important mediators in inflammation and pain, a decrease in mediators involved in cartilage destruction, and an increase in antioxidant activity.(21) It is used in the treatment of many diseases; especially such as chronic low back and neck pain, degenerative joint diseases, soft tissue rheumatism, discopathies and arthralgias. (22-25) There are no comprehensive and adequate studies conducted in patients with symptomatic HR with paraffin administration and peloid therapy. It is thought that peloid and paraffin treatments may have a positive effect on pain, functional status and quality of life in patients with HR. The aim of this study; to investigate the effectiveness of peloid and paraffin treatments on pain, functional status and quality of life in the treatment of symptomatic HR and to compare the results.
In the study, patients who applied to our Health Sciences University Konya Physical Medicine and Rehabilitation polyclinics and were diagnosed with HR clinically and/or radiologically and sent for treatment were examined. Among these patients, 80 patients were included in the study according to the inclusion and exclusion criteria. The patients were divided into two groups of 40 each as peloid therapy and paraffin therapy. Detailed histories of the patients were taken and their sociodemographic and clinical characteristics were recorded. Peloid treatment was given to the first group for 2 weeks, 5 days a week, for a total of 10 sessions. The second group was given paraffin treatment for 2 weeks, 5 days a week, for a total of 10 sessions. A home exercise program including ROM, stretching and strengthening exercises was added to both treatment groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Konya
-
Selçuklu, Konya, Turkey
- Konya Beyhekim Training and Research Hospital Physical Medicine and Rehabilitation Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Pain-limitation in the 1st MTF joint for three months or longer,
- Being over 35 years old,
- 3 or more severe pain according to VAS,
- Localized tenderness over the 1st MTF on palpation.
Exclusion Criteria:
- Having neuropathic or radicular pain,
- History of acute trauma,
- Previous surgical intervention on the foot or non-operative treatment within 6 months (corticosteroid injection, physical therapy applications, shoe modifications, etc.),
- Having rheumatological diseases such as rheumatoid arthritis, psoriatic arthritis, gout,
- Having a malignancy,
- Having a progressive neurological disease that causes sensory defects,
- Being allergic to peloid therapy,
- Being pregnant
- Having a communication problem.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group 1 Peloid treatment
The patients in the first group; Peloid was applied to both feet at 42 °C for 2 weeks, 5 days a week, 10 sessions in total, 20 minutes each session.
|
The patients in the first group; Peloid was applied to both feet at 42 °C for 2 weeks, 5 days a week, 10 sessions in total, 20 minutes each session.
Peloid was applied in a layer of approximately 1.5-2 cm thick, then the foot was wrapped in a nylon bag and covered with a towel.
After 20 minutes of application, the peloid layer was removed and disposed of in medical waste.
The treatment area was cleaned with soft cloths moistened with hot water and the session was ended.
In addition to peloid therapy, a home exercise program including joint range of motion, stretching and strengthening exercises for the 1st MTF with 3 sets of 10 repetitions was described for the patients to do simultaneously.
|
|
Active Comparator: Group 2 Paraffin treatment
The patients in the second group were given paraffin treatment on both feet by dipping method, for 2 weeks, 5 days a week, 10 sessions in total, 20 minutes each session.
|
The patients in the second group were given paraffin treatment on both feet by dipping method, for 2 weeks, 5 days a week, 10 sessions in total, 20 minutes each session.
After the foot was dipped and removed 10 times, it was wrapped in a nylon bag and left for 20 minutes.
Then the paraffin was peeled off the feet and disposed of in medical waste.
Likewise, a home exercise program including joint range of motion, stretching and strengthening exercises for the 1st MTF with 3 sets of 10 repetitions was described for them to do simultaneously.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Descriptive Characteristics of the Patients
Time Frame: Just before the treatment, both groups will be asked in the form of a short questionnaire.
|
A short questionnaire was created to determine the sociodemographic characteristics of the patients.
|
Just before the treatment, both groups will be asked in the form of a short questionnaire.
|
|
Evaluation of Pain Severity
Time Frame: Patients were evaluated just before treatment. (1st measurement)
|
The pain level of the patients was determined by a visual analog scale(VAS).
The patient was asked to mark the value corresponding to resting pain and pain during walking on the scale.
|
Patients were evaluated just before treatment. (1st measurement)
|
|
Evaluation of Functionality and Quality of Life
Time Frame: Patients were evaluated just before treatment. (1st measurement)
|
Foot-ankle outcome score (FAOS) is an international questionnaire used to assess
|
Patients were evaluated just before treatment. (1st measurement)
|
|
Evaluation of Quality of Life
Time Frame: Patients were evaluated just before treatment. (1st measurement)
|
Quality of life was evaluated with the SF-36 health questionnaire.
The SF-36 is a form of 36 questions consisting of 8 subgroups, which is used to measure the general quality of life.
It has eight subscales (general health, physical function, physical condition, pain, life functions, social functions, emotional status, mental health) and 2 specific scales (mental health and physical health).
|
Patients were evaluated just before treatment. (1st measurement)
|
|
Joint Range of Motion Measurement
Time Frame: Patients were evaluated just before treatment. (1st measurement)
|
Dorsiflexion and plantarflexion angles of the 1st MTP joint in both feet of the patients were measured with a goniometer and noted.
In addition, the stages of disease for the patients were determined according to the Coughlin and Shurnas staging system.
|
Patients were evaluated just before treatment. (1st measurement)
|
|
Evaluation of Pain Severity
Time Frame: Patients were evaluated immediately after treatment. (2nd measurement)
|
The pain level of the patients was determined by a visual analog scale(VAS).
The patient was asked to mark the value corresponding to resting pain and pain during walking on the scale.
|
Patients were evaluated immediately after treatment. (2nd measurement)
|
|
Evaluation of Functionality and Quality of Life
Time Frame: Patients were evaluated immediately after treatment. (2nd measurement)
|
Foot-ankle outcome score (FAOS) is an international questionnaire used to assess functionality and quality of life.
The Turkish validity and reliability of this form were studied.
This test consists of 44 questions in total.
Headings include symptoms, pain, work, and daily life, sports, and recreational activities, and quality of life.
|
Patients were evaluated immediately after treatment. (2nd measurement)
|
|
Evaluation of Quality of Life
Time Frame: Patients were evaluated immediately after treatment. (2nd measurement)
|
Quality of life was evaluated with the SF-36 health questionnaire.
The SF-36 is a form of 36 questions consisting of 8 subgroups, which is used to measure the general quality of life.
It has eight subscales (general health, physical function, physical condition, pain, life functions, social functions, emotional status, mental health) and 2 specific scales (mental health and physical health).
|
Patients were evaluated immediately after treatment. (2nd measurement)
|
|
Joint Range of Motion Measurement
Time Frame: Patients were evaluated immediately after treatment. (2nd measurement)
|
Dorsiflexion and plantarflexion angles of the 1st MTP joint in both feet of the patients were measured with a goniometer and noted.
In addition, the stages of disease for the patients were determined according to the Coughlin and Shurnas staging system.
|
Patients were evaluated immediately after treatment. (2nd measurement)
|
|
Evaluation of Pain Severity
Time Frame: The patients were evaluated 1 month after the treatment. (3rd measurement)
|
The pain level of the patients was determined by a visual analog scale(VAS).
The patient was asked to mark the value corresponding to resting pain and pain during walking on the scale.
|
The patients were evaluated 1 month after the treatment. (3rd measurement)
|
|
Evaluation of Functionality and Quality of Life
Time Frame: The patients were evaluated 1 month after the treatment. (3rd measurement)
|
Foot-ankle outcome score (FAOS) is an international questionnaire used to assess functionality and quality of life.
The Turkish validity and reliability of this form were studied.
This test consists of 44 questions in total.
Headings include symptoms, pain, work, and daily life, sports, and recreational activities, and quality of life.
|
The patients were evaluated 1 month after the treatment. (3rd measurement)
|
|
Evaluation of Quality of Life
Time Frame: The patients were evaluated 1 month after the treatment. (3rd measurement)
|
Quality of life was evaluated with the SF-36 health questionnaire.
The SF-36 is a form of 36 questions consisting of 8 subgroups, which is used to measure the general quality of life.
It has eight subscales (general health, physical function, physical condition, pain, life functions, social functions, emotional status, mental health) and 2 specific scales (mental health and physical health).
|
The patients were evaluated 1 month after the treatment. (3rd measurement)
|
|
Joint Range of Motion Measurement
Time Frame: The patients were evaluated 1 month after the treatment. (3rd measurement)
|
Dorsiflexion and plantarflexion angles of the 1st MTP joint in both feet of the patients were measured with a goniometer and noted.
In addition, the stages of disease for the patients were determined according to the Coughlin and Shurnas staging system.
|
The patients were evaluated 1 month after the treatment. (3rd measurement)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: seda çıra, assistant doctor
Publications and helpful links
General Publications
- Wülker NJIA, Zollinger-Kies H: Fußchirurgie. Hallux rigidus. 2004;1:99-103.
- Berlet GC, Hyer CF, Lee TH, Philbin TM, Hartman JF, Wright ML. Interpositional arthroplasty of the first MTP joint using a regenerative tissue matrix for the treatment of advanced hallux rigidus. Foot Ankle Int. 2008 Jan;29(1):10-21. doi: 10.3113/FAI.2008.0010.
- Thermann H, Becher C, Kilger RJTiF, Surgery A. Hallux rigidus treatment with cheilectomy, extensive plantar release, and additional microfracture technique. 2004;3(4):210-5.
- Dülgeroğlu TC, DEMİRKIRAN ND, Erduran M. İleri evre halluks rijiduslu hastalarda yerli üretim total eklem artroplastisi ile tedavi sonuçlarımız. Pamukkale Tıp Dergisi.12(2):215-24.
- Uzunca KJTJoPM, Dergisi RTFTvR. Ayak Bileği ve Ayak Osteoartritleri. 2009;55.
- Coughlin MJ, Shurnas PS. Hallux rigidus. Grading and long-term results of operative treatment. J Bone Joint Surg Am. 2003 Nov;85(11):2072-88.
- Meriç G, Budeyri A, Başdelioğlu K, Demir A, UYSAL AEJBSBD. HALLUKS RİJİDUSTA KULLANILAN TEDAVİ SEÇENEKLERİ.1(2):85-9.
- Zammit GV, Menz HB, Munteanu SE, Landorf KB, Gilheany MF. Interventions for treating osteoarthritis of the big toe joint. Cochrane Database Syst Rev. 2010 Sep 8;(9):CD007809. doi: 10.1002/14651858.CD007809.pub2.
- Polzer H, Polzer S, Brumann M, Mutschler W, Regauer M. Hallux rigidus: Joint preserving alternatives to arthrodesis - a review of the literature. World J Orthop. 2014 Jan 18;5(1):6-13. doi: 10.5312/wjo.v5.i1.6. eCollection 2014 Jan 18.
- Kalish S, Willis FBJTF, Journal AO. Hallux limitus and dynamic splinting: a retrospective series. 2009;2(4):1.
- OKUR SÇ, FİRDİN F, ÖZTÜRK SK, EDEMCİ ŞJBTT, Regülasyon ve Nöral Terapi Dergisi. HALLUKS RİJİDUS TEDAVİSİNDE MANUAL MOBİLİZASYON TEKNİKLERİNİN ETKİNLİĞİNİN DEĞERLENDİRİLMESİ: VAKA SERİSİ.12(3):14-7.
- Kılıçoğlu Ö. Ayak başparmağının hastalıkları: Halluks valgus ve halluks rigidus.
- Stillwell G. General principles of thermotherapy. Therapeutic Heat and Cold: E. Licht New Haven (Conn.); 1965. p. 232-65.
- Oğuz h. Oğuz H, Dursun E, Dursun N, Tıbbi Rehabilitasyon. Öztürk C, Akşit R, Tedavide sıcak ve soğuk. Nobel tıp kitabevi, 2004; 333-353
- UN Ö. Kaplıca Tedavisi. In: Tuna N, Eds. Romatizmal Hastalıklar. Ankara: Hacettepe Taş Kitapçılık; 1994. s. 229-42.
- H. G. Peloidoterapi, Etki, Mekanizması ve Uygulama Yöntemleri. İçinde Karagülle M, editor. Tıbbi Ekoloji ve Hidroklimatoloji. İstanbul: Nobel Tıp Kitabevleri; 2013. 13-18. .
- M.Z. K. Kaplıca Tedavisi, Balneoterapi ve Klimaterapi. İçinde Doğan M Karagülle MZ, editör. Kaplıca Tıbbı ve Türkiye Kaplıca Rehberi. İstanbul: Nobel Tıp kitabevleri. 2002. 1-22.
- MZ K. H G. Peloidler, In: Karagülle MZ (eds). Balneoloji ve Kaplıca Tıbbı, Nobel Tıp Kitabevleri, p: 97-112, İstanbul, 2002 40.
- Odabasi E, Turan M, Erdem H, Tekbas F. Does mud pack treatment have any chemical effect? A randomized controlled clinical study. J Altern Complement Med. 2008 Jun;14(5):559-65. doi: 10.1089/acm.2008.0003.
- Fraioli A, Serio A, Mennuni G, Ceccarelli F, Petraccia L, Fontana M, Grassi M, Valesini G. A study on the efficacy of treatment with mud packs and baths with Sillene mineral water (Chianciano Spa Italy) in patients suffering from knee osteoarthritis. Rheumatol Int. 2011 Oct;31(10):1333-40. doi: 10.1007/s00296-010-1475-5.
- Bellometti S, Richelmi P, Tassoni T, Berte F. Production of matrix metalloproteinases and their inhibitors in osteoarthritic patients undergoing mud bath therapy. Int J Clin Pharmacol Res. 2005;25(2):77-94.
- Codish S, Abu-Shakra M, Flusser D, Friger M, Sukenik S. Mud compress therapy for the hands of patients with rheumatoid arthritis. Rheumatol Int. 2005 Jan;25(1):49-54. doi: 10.1007/s00296-003-0402-4. Epub 2003 Nov 14.
- Flusser D, Abu-Shakra M, Friger M, Codish S, Sukenik S. Therapy with mud compresses for knee osteoarthritis: comparison of natural mud preparations with mineral-depleted mud. J Clin Rheumatol. 2002 Aug;8(4):197-203. doi: 10.1097/00124743-200208000-00003.
- Elkayam O, Ophir J, Brener S, Paran D, Wigler I, Efron D, Even-Paz Z, Politi Y, Yaron M. Immediate and delayed effects of treatment at the Dead Sea in patients with psoriatic arthritis. Rheumatol Int. 2000;19(3):77-82. doi: 10.1007/s002960050107.
- Ardic F, Ozgen M, Aybek H, Rota S, Cubukcu D, Gokgoz A. Effects of balneotherapy on serum IL-1, PGE2 and LTB4 levels in fibromyalgia patients. Rheumatol Int. 2007 Mar;27(5):441-6. doi: 10.1007/s00296-006-0237-x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- beyhekimtrh
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Hallux Rigidus
-
LabrhaCompletedHallux Rigidus, Unspecified FootFrance
-
Oslo University HospitalSorlandet Hospital HFNot yet recruitingHallux Valgus | Hallux Rigidus
-
Hyalex Orthopaedics, Inc.Recruiting
-
Golden Jubilee National HospitalUnknownHallux Valgus | Hallux RigidusUnited Kingdom
-
Tampere University HospitalUnknownHallux Valgus | Hallux RigidusFinland
-
University of Wisconsin, MadisonTerminated
-
University Hospital, GhentWithdrawn
-
Artimplant ABUnknown
-
Rush University Medical CenterMid-America Orthopaedic Association (MAOA)TerminatedHallux Valgus | Hallux RigidusUnited States
-
Nova Scotia Health AuthorityRecruitingHallux Valgus | Hallux RigidusCanada
Clinical Trials on Peloid treatment
-
Konya Meram State HospitalCompletedPatient Engagement | Lateral EpicondylitisTurkey
-
Uşak UniversityRecruitingPain | Otalgia | Temporomandibular Disorders (TMDs)Turkey (Türkiye)
-
Konya Meram State HospitalRecruitingPlantar FasciitisTurkey
-
Fenerbahce UniversityCompleted
-
Gaziosmanpasa Research and Education HospitalCompletedCarpal Tunnel Syndrome (CTS)Turkey (Türkiye)
-
Konya Meram State HospitalRecruitingLateral EpicondylitisTurkey
-
Scientific Center for Family Health and Human Reproduction...Completed
-
Lithuanian University of Health SciencesVersmėEnrolling by invitationOsteoarthritis | Hand Osteoarthritis | Foot OsteoarthritisLithuania
-
Institute of Spa and Balneology, public research...Léčebné lázně Mariánské Lázně a. s.RecruitingKidney Diseases | Urologic Diseases | Nephrolithiasis | Urinary Tract Infections | Nephrocalcinosis | ProstatismCzechia
-
PfizerCompleted